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Academic Abdominal Radiologist - Tufts Medical Center - Boston, MA
Tufts Medicine
location-iconBoston MA

Description: The Department of Radiology at Tufts Medical Center is seeking a 1.0FTE Academic Abdominal Radiologist for a full-time faculty appointment at the rank of Assistant, Associate, or Professor at Tufts University School of Medicine. Why join our team: The Abdominal Imaging Division is a collaborative and inclusive team that interprets abdominal/pelvic radiography, fluoroscopy, ultrasound, CT, and MRI; and there is dedicated academic time and formal mentorship of radiologists that is championed by the Chair who supports the academic mission of excellence in teaching and clinical, translational research. We are a subspecialized academic radiology department with a diverse practice, and we have acquired within the past year 8 new GE ultrasounds, the most advanced CT Siemens scanner, and are acquiring 2 new 3.0T and a 1.5T MRI which will be equipped with the most advanced body MR sequences and the most cutting edge post processing techniques like compressed sensing with deep learning (AI) reconstruction techniques. There will be novel multiparametric prostate MR imaging and advanced liver imaging including elastography, fat quantification and iron quantification. How you will transform patient care: You will have a faculty appointment at Tufts University School of Medicine. You will work with over 20 diagnostic radiology residents and a dedicated body MR fellow. You will join a team of faculty members who are actively engaged in resident and medical student education including teaching conferences, multidisciplinary conferences, and research projects. You will have ample chances to contribute to a team culture that is dedicated to inclusivity, collaboration, innovation, and work life balance. You will have access to the Tufts Clinical and Translational Science Institute to support research initiatives that includes collaborations in Artificial Intelligence with Massachusetts Institute of Technology (MIT) and formal mentorship in grant applications from successfully funded researchers across the medical school faculty. You will have access to New 3.0T MR is being installed this fall with highest gradients, compressed sensing with deep learning (DL) technology, and access to a clinical MR support scientists for works in progress, and an additional 1.5T and 3.0T MR. There are 3 Siemens scanners: two 192 slice dual energy and one, 64 slice with an interventional package, and 8 newly purchased ultrasound machines. Who you are: Completed a Body Imaging Fellowship and be ABR or AOBR certified or eligible. Expertise in CT, MRI, and ultrasound imaging. Knowledge of advanced body MR techniques and spectral CT is a plus. A team player who works cooperatively with a wide range of stakeholders and disciplines that fosters excellence in patient care and enhances patient experience. A radiologist who enjoys teaching residents and supports academic projects/research and who wants to work in an academic environment. COVID-19 Policy: To protect patients, physicians, staff, visitors, and the community from the COVID-19 infection, vaccination for COVID-19 is mandatory for employment unless an exemption is granted for medical or religious reasons. Work, Live, and Grow: Boston, Massachusetts is a dynamic, innovative, and historic city with something for everyone. Whether you seek cultural attractions, an intellectual environment, music and entertainment, museums, night life, shopping, fitness, food festivals, or a sunset harbor cruise- you will find it here. The city of Boston is ideally located in close proximity to the coastal beach towns of Cape Cod and the Berkshires in Western Massachusetts, the White Mountains of New Hampshire, and the Green Mountains of Vermont which offer great summertime recreational activities from swimming, sailing, fishing, hiking, and rock climbing and great winter activities from Nordic skiing to downhill skiing and snowboarding. Boston consistently ranks as one of the most desirable places in the country to live and to raise a family. We pride ourselves on having an inclusive work environment for all of our employees. We offer very competitive salaries and benefits packages including health, dental, and vision insurance and retirement plans. Location: Tufts Medical Center in downtown Boston, Massachusetts. How to apply: You can submit an application via the apply button located at the top of the listing. Should you have any questions regarding the position or any complications submitting an application with us, please feel free to reach out to Ryan Scerra, Senior Provider Recruiter, at ryan.scerra@wellforce.org. Why Wellforce: Tufts Medical Center is a proud member of Wellforce. Wellforce brings together providers and organizations with a shared vision of high-quality care delivered in the setting that serves our patients best. Together, Wellforce brings together the strength of both academic medicine and community care. Diversity, Equity, Inclusion, and Social Responsibility: We truly believe our employees' diverse backgrounds, experiences, and perspectives are a powerful contributor to creative an inclusive environment where everyone can thrive and reach their maximum potential while adding value to both our organization and our patients. We warmly welcome all candidates of diverse origin, background, ability, age, sexual orientation, gender identity, and personality. .Requirements: PI155842323

Full Time
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Bioanalytical Scientist
Absorption Systems
location-iconWoburn MA

Absorption Systems, a preclinical Contract Research Organization is seeking a Bioanalytical Scientist to join the bioanalytical team at our Boston facility.Primary responsibilities include:Assay development, validation, and sample analysis under RUO/GLP/cGMP conditions.Write SOPs, validation protocols, and reports.Serve as a team leader and/or PI and the technical and scientific aspects of development and validation of new assays including GxP studiesMay have direct reports and work as a group leaderAs a team leader, oversee the project timelines and put the best efforts to increase productivity.May represents the company in the scientific conferences or participates in the sales meetingsWork with management and QA to maintain and improve quality systemsProvide leadership and training to assigned research staffProvide high-quality documentation of all lab-related activities, including, for example, assay batch record, sample inventory, etc.Perform a QC function to review data and reports to ensure the accuracy of all laboratory-related processes.Maintain regular communication with the study director and other project staff and become a point of contact to the client.Job Qualifications and Requirements:A minimum of a Bachelor's in a scientific field with 5+ years or an advanced degree (MS/Ph.D.) with at least 3 years of relevant experience.Experience with assay development and validation is required.Experience with ELISA, Western Blot, Luminex, and cell-based assays is critical.Strong experience with GLP and cGMP is required.Ability to quickly acquire new skills and craft creative solutions.Must be detail-oriented with the ability to multi-task and work as part of a team to complete projects with strong communication skills.**Relocation may be available.This Associate Scientist position earns a competitive salary, depending on experience. We also offer a full suite of benefits to choose from, including medical, dental, vision, a health reimbursement account funded by the employer, a healthcare & dependent flexible spending account (FSA), a 401(k) plan, 100%-employer-paid voluntary life/AD&D insurance, and profit-sharing. If this sounds like the right opportunity in pharmaceutical research and cell & gene therapy for you, apply today!BenefitsAbsorption Systems cares about our work community and offers a variety of benefits allowing employees the opportunity to customize a comprehensive benefits package that meets their personal needs.About Absorption Systems, a Pharmaron CompanyAbsorption Systems, founded in 1996, assists pharmaceutical and medical device companies in identifying and overcoming ADMET (Absorption, Distribution, Metabolism, Excretion and Toxicity) barriers in the development of drugs, biologics and medical devices. Additionally, Absorption Systems goes deep into each of those areas, offering in vitro, in situ and in vivo models to assess the properties in question. The company's mission is to continually develop innovative research tools that can be used to accurately predict human outcomes or to explain unanticipated human outcomes when they occur. Absorption Systems has facilities in Exton, PA, San Diego, CA, and Boston, MA to serve customers throughout the world.Alongside of our enthusiasm for science and research, we have a passion to see each and every one of our employees grow and succeed both personally and professionally. We encourage our employees to continually enhance their ability to contribute to the success of the organization and advance their careers. Absorption Systems is committed to creating an environment where individuals are encouraged to grow and work in collaboration with each other while being passionate about innovation. The professional culture of our organization is a goal-oriented environment full of internally driven and motivated professionals. Our company is unique in the fact that there is freedom for autonomy to execute and the ability for each employee to grow in directions that align their individual aspirations with company growth.Absorption Systems is proud to be an Equal Employment Opportunity and Affirmative Action employer.

Full Time
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Scientist or Senior Scientist
Sanofi
location-iconCambridge MA

POSITION OVERVIEW We are seeking an enthusiastic scientist who will be involved in the discovery of novel therapeutics working in Biomarker & Target Engagement Profiling Lab, which is part of Disease Profiling and Functional Genomics Cluster within Precision Medicine and Computational Biology Department. The scientist will contribute to a variety of projects by developing and implementing innovative immunoassay based proteomic methods for identification of biomarkers, disease profiling, and elucidation of drug action mechanisms. In this position, the scientist will also be responsible for evaluation and employment of the emerging cutting-edge proteomic technologies as well as for maintaining operational readiness of the equipment. REQUIRED SKILLS Protein biomarker research - design, validation, and implementation of protein immunoassays: Meso Scale Discovery, ELISA, bead based Simoa, Simple Western etc.Experience in handling biological materials (tissues, tumors, blood samples, CSF, etc.).Lab automation (liquid handling workstations, plate washers).Good knowledge of scientific data analysis, graphing and curve fitting software (Excel, GraphPad Prism, TIBCO Spotfire).Strong organizational and analytical skills; attention to detail is critical.Ability to write technical reports describing experiments and their outcome. BASIC QUALIFICATIONS BS or MS Degree in Biochemistry, Biotechnology or related disciplines with minimum 2 years of experience in protein biomarker assay development and analysis .LOCATION - Cambridge At Sanofi R&D North America, we deliver meaningful solutions for patients. We transform science into breakthrough, best-in-class and first-in-class medicines and vaccines. We believe in creating a diverse and inclusive workforce - and workplace - which brings together the collective brainpower of over 2,000 colleagues and provides you with an exciting place to grow and develop. We set the bar high, and we deliver. Join us and together we will build on our trusted legacy of breakthroughs for society. Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law. As a healthcare company and a vaccine manufacturer, Sanofi has an important responsibility to protect individual and public health. All US based roles require individuals to be fully vaccinated against COVID-19 as part of your job responsibilities. According to the CDC, an individual is considered to be "fully vaccinated" fourteen (14) days after receiving (a) the second dose of the Moderna or Pfizer vaccine, or (b) the single dose of the J&J vaccine. Fully vaccinated, for new Sanofi employees, is to be fully vaccinated 14 DAYS PRIOR TO START DATE. At Sanofi diversity and inclusion is foundational to how we operate and embedded in our Core Values. We recognize to truly tap into the richness diversity brings we must lead with inclusion and have a workplace where those differences can thrive and be leveraged to empower the lives of our colleagues, patients and customers. We respect and celebrate the diversity of our people, their backgrounds and experiences and provide equal opportunity for all.

Full Time
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ACCOUNT EXECUTIVE (full-time with commission plan)
Safety NetAccess Inc
location-iconBoston MA

Job Description *Safety NetAccess is now hiring Account Executives who are passionate about providing superior customer service and focused on delivering results to join the sales team. Candidate must be willing to travel for a client visit*Job Type: Full Time / Remote (travel is a must for client visit)Work Location: RemoteResponsibilities:Prospecting, creating new relationships, and closing businessDeveloping and executing targeted strategies for growthCreating customer-centric quotations & proposalsEstablishing and maintaining new accounts and distribution channelsDelivering the highest quality of customer service Qualifications:Must have a Post-secondary educationExperience in Hospitality industry is an advantageTechnically perceptive with superior communication skillsPrevious technical sales solution sales experienceStrong administration and organization skillsComputer skills & aptitude – experienced with online demonstrations and tracking software (CRM)Self-motivated, deadline and bottom line drivenKnowledge of business organization structures, buying influences, and purchasing processesMust have a valid passportAbout Safety NetAccess:Many companies do what we do. But no one else does it like we do. Because for us, it’s personal. Since 2001, Safety NetAccess has been designing, building and supporting wireless networks for hotels, resorts and other public properties. We’ve grown from a two-man start-up to one of the country’s most trusted providers, and yet we still feel like we’re just getting started. Along the way, we have been certified by Marriott Hotels, are a preferred vendor for Wyndham Hotels, and an endorsed vendor for Best Western Hotels. Today, Safety NetAccess is deployed in 4,000+ venues providing millions of authentications daily, and while we are proud of our growth and the distinctions received, what truly excites us is thinking about the millions of users who have had a flawless experience with our networks.Perks and Benefits:Challenging and exciting work with a collaborative teamCommission Plan Health, Dental, Life, Short Term, and Long Term Disability insuranceGenerous paid time offCompany Holidays401K with company matchingWe thank all applicants for their interest. Only those selected for interviews will be contacted.Find us on:Facebook - https://www.facebook.com/safetynetaccessTwitter - https://twitter.com/safetynetaccessLinkedIn - https://www.linkedin.com/company/safetynetaccessinc/Company Website - https://www.safetynetaccess.com/

Full Time
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Scientist, In vitro iPSC culture and differentiation
Pfizer
location-iconCambridge MA

Why Patients Need YouPfizer s purpose is to deliver breakthroughs that change patients lives. Research and Development is at the heart of fulfilling Pfizer s purpose as we work to translate advanced science and technologies into the therapies and vaccines that matter most. Whether you are in the discovery sciences, ensuring drug safety and efficacy or supporting clinical trials, you will apply cutting edge design and process development capabilities to accelerate and bring the best in class medicines to patients around the world.As a Scientist, you will be at the center of our operations and you ll find that everything we do, every day, is in line with an unwavering commitment to quality. You will be part of a team that is addressing the critical task of rejuvenating our pipeline with innovative, differentiated First-In-Class/ Only-In-Class programs in the years to come. This will be addressed by generation of strong data packages from target hypotheses derived from academic outreach and initiatives. You will be an essential member of this team and creatively design and execute key experiments to address the basic and translational biology of novel drug targets, their molecular pathways, and their connection to human disease.With your deep knowledge in the discipline, you will be an active team member who influences at the project team level. You will be using your scientific judgment to adapt standard methods and techniques by applying prior work experience and consulting others. Your ability to plan will help in preparing short-term work activities on projects. Your creativity in developing novel processes and new ideas will be used frequently. You will undertake mentoring activities to guide your team members.It is your innovative scientific temperament that will help in making Pfizer ready to achieve new milestones and help patients across the globe.What You Will AchievePfizer s Rare Disease Research Unit (RDRU) is focused on developing therapies for rare inherited diseases, including rare cardiac diseases.The successful candidate will be a member of the rare cardiac disease research group. The role s primary responsibility will be to contribute to the production and characterization of iPSC-derived cardiomyocytes to support our rare cardiology portfolio. The preferred candidate would have hands-on experience with the maintenance of pluripotent stem cells (iPS or ES) and their differentiation into relevant cell types including cardiomyocytes.The candidate is expected to have excellent critical thinking, problem-solving, and presentation skills (written and oral) and will need to effectively communicate with internal partners.How You Will Achieve ItContribute to the achievement of goals of the team and influence at the work group/project team level.Apply technical skills and functional knowledge to projects/ assignments within own work group/ project team independently and proactively.Perform laboratory experiments to help establish robust disease biology, biochemical and cell-based compound screening assays and carry out in vivo evaluation across a broad array of target classes for the project teams.Prepare and present experimental results to project teams.Comply with all safety training and good laboratory practices.Propagate and maintain iPSC cultures and iPSC-derived cell cultures for program advancement, with an immediate focus on cardiomyocytesPerform characterization and validation of iPSC cardiomyocytes using various approaches such as ELISA, qRT-PCR, FACS, Western blotting, and immunostainingDevelop Standard Operating Procedures for the maintenance, differentiation, and banking of different patient-derived iPSCsPerform experimental studies, conduct data analysis and interpretation, record results in an electronic lab notebook, and stay abreast of novel relevant findings from the literatureHelp to identify, evaluate, and implement novel methods or technologies that would enhance workflow efficiencies and/or improve the quality of cell reagent deliverablesBe highly motivated, organized and show significant ability to work effectively and collaboratively in a team-oriented environment as a part of the Rare Disease biology group to advance our pipeline of candidate therapies.QualificationsMust-HaveB.S. or M.S. in a relevant disciplineAt least 6 years of laboratory experience in academia or industry for B.S. and 4 years for M.S.Hands-on experience with undifferentiated iPSC culture, including expansion, banking, and quality controlExperience with differentiation and characterization of iPSCs, with preference towards cardiomyocytesMolecular biology skills including mammalian cell DNA/RNA extraction and PCR/RT-PCR/qPCRFamiliarity with cellular biology techniques including immunocytochemistry, high-content imaging, image analysis, western blot, cell-based assaysAbility to execute, troubleshoot and analyze experiments and interpret resultsPrecise documentation of procedures and results in compliance with Electronic Lab Notebook guidelinesStrong interpersonal and organizational skillsGood oral and written communication skillsMust be willing to work with cells of human originNice-to-HaveExperience analyzing cardiomyocyte functionExperience with cell transfection and AAV transductionPHYSICAL/MENTAL REQUIREMENTSWill require standard laboratory physical workPfizer requires all U.S. new hires to be fully vaccinated for COVID-19 prior to the first date of employment. As required by applicable law, Pfizer will consider requests for Reasonable Accommodations.Sunshine ActPfizer reports payments and other transfers of value to health care providers as required by federal and state transparency laws and implementing regulations. These laws and regulations require Pfizer to provide government agencies with information such as a health care provider s name, address and the type of payments or other value received, generally for public disclosure. Subject to further legal review and statutory or regulatory clarification, which Pfizer intends to pursue, reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act. Therefore, if you are a licensed physician who incurs recruiting expenses as a result of interviewing with Pfizer that we pay or reimburse, your name, address and the amount of payments made currently will be reported to the government. If you have questions regarding this matter, please do not hesitate to contact your Talent Acquisition representative.EEO & Employment EligibilityPfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status. Pfizer also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA. Pfizer is an E-Verify employer.Research and Development

Full Time
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Associate Scientist - Discovery Research
Novo Nordisk
location-iconLexington MA

About the Department Dicerna, a Novo Nordisk company, is focused on driving innovation in RNAi (ribonucleic acid interference) to selectively target and silence genes that cause or contribute to disease. Our proprietary GalXC and GalXC-Plus RNAi technologies have the potential to address conditions that are difficult or impossible to treat with other modalities. Established as a Transformational Research Unit (TRU) following Novo Nordisk s acquisition of Dicerna Pharmaceuticals, Inc. in December 2021, the Dicerna TRU is a unique new organization within Novo Nordisk that brings together the best of both worlds - the agility, collaborative pioneering spirit and calculated risk-taking profile of a biotech along with the scale, resources and capabilities of a global leader in drug development. With approximately 200 researchers, scientists, drug developers and operational staff, we are a team of inventive and entrepreneurial thinkers pushing the boundaries of science to create and drive new RNAi-based therapies for both rare and more prevalent diseases from the bench to the clinic. Together, we are driving change. Are you ready to make a difference? The Position The Discovery Research team is looking for a highly motivated Research Associate/Associate Scientist to help with the discovery and development of GalXC-Plus RNAi therapeutics. This candidate will be responsible for helping prosecute in vivo and in vitro studies exploring the pharmacodynamics and efficacy for novel RNAi therapeutics and to advance the GalXC and GalXC-Plus platforms. The ideal candidate is a self-starter who is eager to learn, highly collaborative, and detail oriented. The successful candidate will be asked to carry out experiments and analysis in a manner reflecting an organization that demands scientific rigor and technical excellence with training and mentorship from a Scientist. Applicants interested in oligonucleotide therapeutics, gene therapy, or pharmaceutical sciences are encouraged to apply. Relationships This role will report to a Scientist II in Discovery Research. Essential Functions Laboratory Techniques: Tissue sample processing (protein and mRNA) for downstream bioassays Generating and analyzing molecular assay data using a variety of methodologies (examples: quantitative imaging, qRT-PCR, plate-based assays, enzyme assays) with rigorous scientific standards, troubleshooting where needed, and careful documentation practices In-life operations: Rodent dosing, sampling and necropsy; collaborating cross-functionally to promote efficient operations in a high-volume on-site animal care facility (ACF) Development, validation, optimization, and troubleshooting of molecular endpoint bioassays Additional Responsibilities Careful documentation practices, i.e., maintenance of electronic laboratory notebooks Data package preparation and presentation Participation in team and departmental meetings Cross-functional communication Physical Requirements 0-10% overnight travel required. Ability to lift 0-10 lbs. Qualifications BS/MS in Biology, Biochemistry, Pharmaceutical Sciences or equivalent 1+ years of relevant laboratory experience in an appropriate industrial or academic environment Experience in downstream bioassays including one or more of the following: qPCR, ELISA/Western blot, IHC Practical knowledge in basic biochemical and molecular biology principles including RNAi theory/practice Preferred: Experience in rodent pharmacology including dosing and necropsy; familiarity with PK/PD concepts Commitment to careful and thorough technical documentation, including electronic laboratory notebooks and study reports Strong organizational, IT and communication skills; ability to interact effectively on multidisciplinary teams and participate in our dynamic company culture Ability to multitask and prioritize (Title and compensation based on experience level) We commit to an inclusive recruitment process and equality of opportunity for all our job applicants. At Novo Nordisk we recognize that it is no longer good enough to aspire to be the best company in the world. We need to aspire to be the best company for the world and we know that this is only possible with talented employees with diverse perspectives, backgrounds and cultures. We are therefore committed to creating an inclusive culture that celebrates the diversity of our employees, the patients we serve and communities we operate in. Together, we re life changing. Novo Nordisk is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, protected veteran status or any other characteristic protected by local, state or federal laws, rules or regulations. Novo Nordisk requires all new hires to be fully vaccinated against COVID-19 prior to the first date of employment. As required by applicable law, Novo Nordisk will consider requests for reasonable accommodation. If you are interested in applying to Novo Nordisk and need special assistance or an accommodation to apply, please call us at 1-. This contact is for accommodation requests only and cannot be used to inquire about the status of applications. Print job Send to email

Full Time
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Scientist I- Oncology
Takeda Pharmaceutical
location-iconBoston MA

By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice and Terms of Use. I further attest that all information I submit in my employment application is true to the best of my knowledge.Job DescriptionAbout the role:Our vision is to be a forward-looking, world-class R&D organization that unlocks innovation and delivers transformative therapies to patients.Join Takeda as a Scientist I where you will contribute to and implement new ideas with in vitro and in vivo proof of concept studies to enable initiation of new discovery project concepts. As part of the Oncology Drug Discovery Unit, you will report to one of our Senior Scientists.How you will contribute:Partner with teams to implement decision allowing preclinical experiments to better understand mechanisms of action of novel therapeuticsIndependently and collaboratively design, validate, and implement a variety of assays to understand biology associated with targets of interest for I/O applicationsUse technical literature to implement novel procedures, changes, and improvements within a project. Can duplicate and modify experimental procedures based on the literatureHelp execute specific research procedures, coordinating schedules of experiments and procedures (~75% of time in the laboratory).Compile data from complex experiments, implement analysis and communicate findings through presentation formatPresent comprehensive technical or project reports and formal presentations /posters to full range of our audiencesMinimum Requirements/Qualifications:PhD degree in a scientific discipline (no post doc experience required) , or MS with 4+ years experience, or BS with 6+ years experience.Demonstrate knowledge of immunological principles including prior experience carrying out data acquisition, analysis and interpretation of molecular or cell-based assays and in vivo experimentsIndependence with multiplexing immune profiling platforms (cell separation, sterile culture, multi-dimension Flow cytometry, Luminex, MSD).Independence in protein analytical methods (ELISA, Western Blotting).Independence in molecular biology applications (DNA/RNA prep, qPCR, nanostring)What Takeda can offer you:Comprehensive Healthcare: Medical, Dental, and VisionFinancial Planning & Stability: 401(k) with company match and Annual Retirement Contribution PlanHealth & Wellness programs including onsite flu shots and health screeningsGenerous time off for vacation and the option to purchase additional vacation daysCommunity Outreach Programs and company match of charitable contributionsFamily Planning SupportFlexible Work PathsTuition reimbursementMore about us:At Takeda, we are transforming patient care through the development of novel specialty pharmaceuticals and best in class patient support programs. Takeda is a patient-focused company that will inspire and empower you to grow through life-changing work.Certified as a Global Top Employer, Takeda offers stimulating careers, encourages innovation, and strives for excellence in everything we do. We foster an inclusive, collaborative workplace, in which our teams are united by an unwavering commitment to deliver Better Health and a Brighter Future to people around the world.Absent an approved religious or medical reason, all US office-based and lab-based Takeda employees who work fully on-site or in a hybrid model (as determined by Takeda) must be fully vaccinated to work at a Takeda site or to engage with Takeda colleagues or anyone else on behalf of Takeda. US field-based employees must be fully vaccinated as a condition of employment, absent an approved religious or medical reason. US employees who work at a Takeda manufacturing facility, and those who work at a BioLife center or BioLife lab, may be subject to different guidelines. If you are contacted by a Takeda recruiter about your job application, we encourage you to seek more information on the applicable guidelines for the Business Unit/Function to which you have applied.In accordance with the CO Equal Pay Act, Colorado Applicants Are Not Permitted to ApplyEEO StatementTakeda is proud in its commitment to creating a diverse workforce and providing equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, gender expression, parental status, national origin, age, disability, citizenship status, genetic information or characteristics, marital status, status as a Vietnam era veteran, special disabled veteran, or other protected veteran in accordance with applicable federal, state and local laws, and any other characteristic protected by law.LocationsBoston, MAWorker TypeEmployeeWorker Sub-TypeRegularTime TypeFull time

Full Time
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Scientist I - Translational Biology
Novo Nordisk
location-iconLexington MA

About the Department Dicerna, a Novo Nordisk company, is focused on driving innovation in RNAi (ribonucleic acid interference) to selectively target and silence genes that cause or contribute to disease. Our proprietary GalXC and GalXC-Plus RNAi technologies have the potential to address conditions that are difficult or impossible to treat with other modalities. Established as a Transformational Research Unit (TRU) following Novo Nordisk s acquisition of Dicerna Pharmaceuticals, Inc. in December 2021, the Dicerna TRU is a unique new organization within Novo Nordisk that brings together the best of both worlds - the agility, collaborative pioneering spirit and calculated risk-taking profile of a biotech along with the scale, resources and capabilities of a global leader in drug development. With approximately 200 researchers, scientists, drug developers and operational staff, we are a team of inventive and entrepreneurial thinkers pushing the boundaries of science to create and drive new RNAi-based therapies for both rare and more prevalent diseases from the bench to the clinic. Together, we are driving change. Are you ready to make a difference? The Position We are seeking an individual to fill the Scientist, Translational Biology role as it is a key member of Dicerna s Biology teams, who will engage in multiple internal and partnered research and discovery efforts that aim to develop therapeutics to treat patients with rare and common diseases. We are seeking a highly skilled scientist with experience in target identification capable of identifying mechanism-of-action and conducting pharmacology studies. Primary responsibilities will include the design, management, and execution of in vivo animal models of disease to evaluate the efficacy, pharmacodynamics, and mechanisms of action of pre-clinical and clinical drug candidates. The successful candidate will interact closely with members of Translational Biology and other groups within Dicerna. You will apply your expertise in animal models and deep understanding of molecular and cellular biology to study liver and other diseases and play a key role in all phases of drug discovery and clinical development at Dicerna. Relationships Reports to Director, Translational Biology. Essential Functions Provide scientific and technical ability to assess new target and therapeutic hypotheses for the Translational Biology group Conduct efficacy, pharmacokinetics, pharmacodynamics, structure-activity-relationship and mechanisms of action studies of siRNA drug candidates Use appropriate in vivo models to understand the mechanisms by which our drug candidates may contribute to efficacy and potential adverse events in patients Present working progress to team members in a group meeting Work closely with Dicerna s research team members to develop molecular and cellular assays to quickly and effectively address key questions related to the safety and efficacy of our drugs Review literature and provide insights to research directions, while making hands-on contributions to the research Develop in vivo model systems and technologies to evaluate efficacy, pharmacodynamics, and mechanisms of action of drug candidates Serve as a role model for compliant behavior that is consistent with the mission, vision and values of the Dicerna organization Physical Requirements Approximately 0 - 10% overnight travel. Ability to lift 0 - 10lbs Qualifications PhD in Biology, Cell or Molecular Biology, or a related field, ideally with a >3 years industry experience Experience in designing and performing molecular and cellular biology techniques, including but not limited to administration of test compounds, collecting tissue samples RNA preparation, RT-qPCR, ELISA, immunohistochemistry, western blot In depth knowledge of, and hands-on experience with, in vitro and in vivo models used for mechanistic investigation and new target identification A true team player with high degree of energy and a passion for contributing to the discovery and development of novel therapeutics A mentor and coach for more junior people who might be reporting to you or others in the group Excellent verbal and written communication skills A documented and strong ability to collaborate with colleagues productively in a fast-paced environment We commit to an inclusive recruitment process and equality of opportunity for all our job applicants. At Novo Nordisk we recognize that it is no longer good enough to aspire to be the best company in the world. We need to aspire to be the best company for the world and we know that this is only possible with talented employees with diverse perspectives, backgrounds and cultures. We are therefore committed to creating an inclusive culture that celebrates the diversity of our employees, the patients we serve and communities we operate in. Together, we re life changing. Novo Nordisk is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, protected veteran status or any other characteristic protected by local, state or federal laws, rules or regulations. Novo Nordisk requires all new hires to be fully vaccinated against COVID-19 prior to the first date of employment. As required by applicable law, Novo Nordisk will consider requests for reasonable accommodation. If you are interested in applying to Novo Nordisk and need special assistance or an accommodation to apply, please call us at 1-. This contact is for accommodation requests only and cannot be used to inquire about the status of applications. Print job Send to email

Full Time
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Scientist, Genomic Medicine Bioanalytics, Cellular Therapies
Sanofi
location-iconWaltham MA

Position Overview/Department Description Sanofi is seeking a highly motivated Scientist to join the Analytical Development team in our growing Genomic Medicines Unit (GMU) in Waltham, MA. The candidate will play a critical role in the design and development of cell-based potency and immunological assays to support product characterization studies, process development, and preclinical and clinical lot release and stability testing of viral and non-viral gene therapeutics, including LNP/mRNA/DNA modalities. A successful candidate will have a strong scientific background in cell-based assay and immunoassay development, excellent oral and written communication skills, and a team player approach to problem-solving.Job Responsibilities:Define scientific approaches and analysis methods for quantitative bioassays, immunoassays, and molecular assaysEvaluate and implement new technologies within the GMU Analytical Development Team, with an emphasis on state-of-the-art immunology, cell-based, and analytical assaysParticipate in the development, qualification and validation of bioassays and immunoassays.Ensure timely completion and delivery of analytical results and documentation to support product development during clinical phases.Write analytical sections of IND/IMPD filingsWrite and review method protocols, assay qualification and validation plans/reports and ensure that the documents adhere to GxP requirements and ICH guidelines.Basic Qualifications:PhD in Biological Sciences (Cell Biology, Biochemistry, Immunology or related field) with a minimum of 0 - 2 years of relevant industry experience, or Master s Degree in a relevant discipline and at least 4 years of relevant experience, or Bachelor s Degree in relevant discipline and at least 6 years of relevant experience.Experience in developing and analyzing quantitative cell-based and biochemical/immunological assays in the context of relative potency.Preferred Qualifications:Understanding of MOA for protein, antibody and gene therapy-based therapeutics.Experience with flow cytometry, PCR, ELISA, western blotting, cell-based cytotoxicity/proliferation assays, and affinity/ligand platforms such as surface plasmon resonance.Familiarity with software packages to analyze dose-responses and statistical analysis (SoftMax, JMP, etc).Familiar with QbD principles and DOE approaches for method development and optimization.Working experience in GMP environment will be considered an advantage.Experience with validation and transfer analytical methods. At Sanofi R&D North America, we deliver meaningful solutions for patients. We transform science into breakthrough, best-in-class and first-in-class medicines and vaccines. We believe in creating a diverse and inclusive workforce - and workplace - which brings together the collective brainpower of over 2,000 colleagues and provides you with an exciting place to grow and develop. We set the bar high, and we deliver. Join us and together we will build on our trusted legacy of breakthroughs for society. Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law As a healthcare company and a vaccine manufacturer, Sanofi has an important responsibility to protect individual and public health. All US based roles require individuals to be fully vaccinated against COVID-19 as part of your job responsibilities. At Sanofi diversity and inclusion is foundational to how we operate and embedded in our Core Values. We recognize to truly tap into the richness diversity brings we must lead with inclusion and have a workplace where those differences can thrive and be leveraged to empower the lives of our colleagues, patients and customers. We respect and celebrate the diversity of our people, their backgrounds and experiences and provide equal opportunity for all.

Full Time
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Research Associate/Sr. Research Associate, Chemical Biology - Boston
Frontier Medicines
location-iconBoston MA

Job DescriptionFrontier Medicines is seeking a highly motivated Research Associate/Senior Research Associate with expertise in proteomics and mass spectrometry to join the Frontier Medicines Chemical Biology group. The successful candidate will be responsible for performing chemical biology assays across a variety of disciplines and techniques to drive drug discovery. Experience with activity-based protein profiling and chemoproteomics is highly desirable.This individual will work closely with an experienced team of interdisciplinary scientists and have regular opportunities to present findings to the project team and senior management. The candidate should have a strong desire to learn new techniques and the ability to incorporate new methodologies into their work. The ideal candidate will be self-driven, resourceful, organized, focused, and enjoy working in a dynamic team environment driven to deliver quality data to enable drug discovery. This position is located in our Boston office.RequirementsWhat you will do: Execute mass spectrometry-based assays for lead identification, optimization, and characterization with a high level of independence.Develop and execute activity-based protein profiling assays for target-engagement assessment and selectivity profiling (gel-based, proteomics, etc).Troubleshoot and optimize experiments to ensure generation of high-quality data.Routinely use automation and liquid-handlers to execute key assays. Analyze data and provide updates to project teams while meeting strict timelines and goals.Maintain a clear, detailed laboratory notebook to document all experiments and findings.Comply with best laboratory safety practices.What we are looking for: B.S. or Masters degree in Chemical Biology/Biochemistry, Chemistry, Cell/Molecular Biology, or related field with 2+ years industry/academic lab experience preferred.Hands-on expertise with liquid chromatography and mass spectrometry is preferred. LC/MS experience with intact protein characterization, enzymatic digestion/lysate characterization, TMT proteomics, activity-based protein profiling, etc is highly desirable.Experience with chemical biology/biochemistry techniques such as gel electrophoresis and western blot is highly desirable.Experience with liquid-handling and automation is highly desirable. The candidate should be driven, have a desire to work in a cross-disciplinary team, and thrive in a dynamic start-up environment.Excellent communication, organization, time management, and technical writing skills.Strong problem-solving skills and ability/desire to learn new skills.Research Associate level will be determined based on level of experience.Legally authorized to work in the US.BenefitsHealth Care Plan (Medical, Dental & Vision)Retirement Plan (401k, IRA)Life Insurance (Basic, Voluntary & AD&D)Paid Time Off (Vacation, Sick & Public Holidays)Family Leave (Maternity, Paternity)Short Term & Long Term DisabilityTraining & DevelopmentFree Food & SnacksWellness ResourcesStock Option Plan

Full Time
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mRNA Analytical Development Head of Bioassay
Sanofi
location-iconWaltham MA

In the race for the future of health - The Sanofi MRNA Center of Excellence (CoE) At Sanofi, we chase the miracles of science, and we know mRNA has a role to play in the future of health. And while the pandemic has shaken up our industry, creating new opportunities and risks, we believe the acceleration of innovation with mRNA technology means vaccines and treatments for more people faster than before. That s why we re looking for bold, optimistic world-changers to join our mRNA Center of Excellence. We re investing €400m a year into the new Center, hiring a team of 450 dedicated employees, and focusing on implementing an integrated end-to-end mRNA vaccine capabilities and research with R&D, digital and CMC teams. Bring your ambition and optimism and join us on our journey to discover and deliver transformative medicine to patients through the advancement of our cutting-edge mRNA technology! About the Opportunity Sanofi Pasteur is looking for a skilled and highly motivated individual with expertise in physicochemical and biochemical methods development to develop novel methods and improve characterization of mRNA vaccines in development by working closely with the bioprocess development group.Analytical Sciences Department has the overall responsibility to develop, qualify and validate robust analytical methods to support release and characterization testing of mRNA Drug Substances and Drug Products candidates in development. Core Responsibilities Lead the analytical development Bioassay team to support all analytical CMC activities for mRNA-based vaccine and drug development from Phase 1 to phase 3, including but not limit to process development, analytical release stability and characterization testing, CRO management, documentation management, and regulatory submission, etc. Represent the Analytical Science group in CMC teams.Plan, initiate, and direct the overall scientific activities for new projects including new technological ideas.Engage in bench laboratory work when appropriate, e.g., developing new bioassay methods for mRNA vaccine development, e.g., including cell-based western blot, sanger sequencing, high throughout sequencing, ELISA, qPCR, ddPCR, endotoxin and microbiology assays, binding assays, kinetic assays, etc.Set the scientific standards. Develop and author complex, explicit documentation for new and current procedures, validation protocols and technical reports incorporating appropriate use of statistics.Stay current with regulatory guidance for vaccine and biological drug development and serves as a thoughtful leader and internal expert in dealing with regulatory commitments and responses.Initiate complex projects, which have significant scientific risk and applies strong scientific risk assessment skills.Develop innovative and relevant solutions to extremely complex problems.Make critical contributions to scientific literature and conferences and is recognized internally and externally at national and international levels.Oversee analytical method development, qualification, validation, and transfer.Identify potential problems and proactively suggest technical solutions based upon analytical expertise and knowledge of product/process. Function in a project leadership role, guiding the successful completion of major projects to meet the projected timeline.Participate in project strategy in consultation with supervisor and/or colleagues.Lead the analytical CMC section writing for regulatory submissions and responses.Work under consultative direction toward long-range goals and objectives. Assignments are often self-initiated.Represent the organization in providing solutions to difficult technical issues associated with specific projects.Manage and direct the work of analysts and scientists. Interact with senior external personnel on significant technical matters often requiring coordination between organizations.Serve as organization spokesperson on advanced projects and/or programs. Act as advisor to management and/or customers on advanced technical research studies and applications.Leadership SkillsAn ongoing commitment to conducting our global business according to the highest legal and ethical standards, and to continually pursue excellence in the development and delivery of all of our products and services. This includes:Respecting the laws and operating within the applicable regulations of the places in which we conduct business, as well as our own Company policies and procedures.Being honest and treating people with respect and courtesy.Constantly striving to make Sanofi a great place to work, and a company respected for the quality of its people and products.Acting as role models for our fellow employees by acting responsibly, fairly, and honestly in our dealings and exercising sound judgment in performing our jobs.Leading PeopleSanofi's leaders motivate, inspire, build, and retain highly effective manufacturing teams while managing for high performance and developing others. They are versatile learners and courageous decision makers.Leading the BusinessSanofi's leaders are effective operating in an evolving, complex and dynamic environment, providing clear direction and instruction to direct reports, and continuously looking internally and externally for best practices and areas for improvement.Delivering to CustomersSanofi's leaders understand patient and customer needs and build relationships as required to meet manufacturing goals while continuously improving operations by setting high standards for the team so they may perform to a level of excellence. Competencies / Requirements PhD or MSc/degree in Cell biology, Biology, Microbiology or related sciences.PhD with 8+ years or MSc with at least 12+ of pharma/biotech industry experience, skilled in analytical bioassays.Demonstrated people and project leadership skills.Ability to perform complex method development and propose appropriate method improvement.Knowledge of nucleic acid/oligonucleotides chemistry and standard analytical methods of these molecules.Experience in various biological and bioanalytical assays, including cell-based western blot, sanger sequencing, high throughout sequencing, ELISA, qPCR, ddPCR, endotoxin and microbiology assays, binding assays, kinetic assays, etc.Thorough understanding of analytical technology and relevant statistical methods. Proven capability of evaluating/developing new technologies.Excellent organizational skills.Significant amount of regulatory knowledge and guidance in cGMP, ICH, USP, etc. Able to work independently and collaborate in teams, enthusiastic and self-motivated. Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law. As a healthcare company and a vaccine manufacturer, Sanofi has an important responsibility to protect individual and public health. All US based roles require individuals to be fully vaccinated against COVID-19 as part of your job responsibilities. According to the CDC, an individual is considered to be "fully vaccinated" fourteen (14) days after receiving (a) the second dose of the Moderna or Pfizer vaccine, or (b) the single dose of the J&J vaccine. Fully vaccinated, for new Sanofi employees, is to be fully vaccinated 14 DAYS PRIOR TO START DATE. At Sanofi diversity and inclusion is foundational to how we operate and embedded in our Core Values. We recognize to truly tap into the richness diversity brings we must lead with inclusion and have a workplace where those differences can thrive and be leveraged to empower the lives of our colleagues, patients and customers. We respect and celebrate the diversity of our people, their backgrounds and experiences and provide equal opportunity for all.

Full Time
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CDL-A Lease Purchase Truck Driver - Take Home $1,500+ weekly!
Western Express
location-iconChelsea MA

CALL TO SPEAK WITH A SEATING SPECIALIST TODAY!(888) 981-4222Have you ever dreamed of owning your truck and being your own boss? Come experience the many reasons why Western Express is the best place to live out those dreams!This program was built for you to succeed, become an owner operator, and own your future.Western Express is now offering a wide variety of new and used trucks, so you can find the one that is right to call your own. With no money down, no credit check and no balloon payment, this walk-away lease is simply the best ownership program in the industry.***$2,500 SIGN-ON BONUS***We Offer:REAL RATES – Up to $2.00 per mile + industry-leading fuel surcharge on ALL MILES!GO BIG – $1,500/week median settlements AFTER expenses; Top Earners net $4,000+!GO HOME – No Forced Dispatch; Choose your Home Time!Great Selection of New and Used TrucksLow Weekly Payments (Between $575 - $745/week!)No Money Down, No Interest, No Balloon Payment, No Credit Check!Ownership in 3-5 years (depending on year/make/model selected)Business Tools and Guidance to help you manage and grow your businessAccess to some of the most inexpensive Insurance in the industryBig Discounts on Fuel and TiresBestPass to cover all Toll Expenses24/7 Operations and Maintenance Support$2,500 Sign-On Bonus!INTERESTED IN BEING A DRIVER TRAINER? Drive for us for 3 months or more and you can qualify as a driver trainer at Western Express! Call today for more details on how you can add up to 50% to your revenue!Have you been out of driving for 3 years or more? Are you a recent CDL-A grad? Call us for information about our Training Programs today!Requirements:Valid CDL-A (no experience required)21 Years of Age or OlderWestern Express is a non-discriminatory and equal opportunity employer. Regardless of background, we'd like to speak with you to see if you qualify.*Subject to change without notice. Some restrictions may apply. Call for details.

Full Time
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CDL-A Lease Purchase Truck Driver - Take Home $1,500+ weekly!
Western Express
location-iconCambridge MA

CALL TO SPEAK WITH A SEATING SPECIALIST TODAY!(888) 981-4222Have you ever dreamed of owning your truck and being your own boss? Come experience the many reasons why Western Express is the best place to live out those dreams!This program was built for you to succeed, become an owner operator, and own your future.Western Express is now offering a wide variety of new and used trucks, so you can find the one that is right to call your own. With no money down, no credit check and no balloon payment, this walk-away lease is simply the best ownership program in the industry.***$2,500 SIGN-ON BONUS***We Offer:REAL RATES – Up to $2.00 per mile + industry-leading fuel surcharge on ALL MILES!GO BIG – $1,500/week median settlements AFTER expenses; Top Earners net $4,000+!GO HOME – No Forced Dispatch; Choose your Home Time!Great Selection of New and Used TrucksLow Weekly Payments (Between $575 - $745/week!)No Money Down, No Interest, No Balloon Payment, No Credit Check!Ownership in 3-5 years (depending on year/make/model selected)Business Tools and Guidance to help you manage and grow your businessAccess to some of the most inexpensive Insurance in the industryBig Discounts on Fuel and TiresBestPass to cover all Toll Expenses24/7 Operations and Maintenance Support$2,500 Sign-On Bonus!INTERESTED IN BEING A DRIVER TRAINER? Drive for us for 3 months or more and you can qualify as a driver trainer at Western Express! Call today for more details on how you can add up to 50% to your revenue!Have you been out of driving for 3 years or more? Are you a recent CDL-A grad? Call us for information about our Training Programs today!Requirements:Valid CDL-A (no experience required)21 Years of Age or OlderWestern Express is a non-discriminatory and equal opportunity employer. Regardless of background, we'd like to speak with you to see if you qualify.*Subject to change without notice. Some restrictions may apply. Call for details.

Full Time
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CDL-A Lease Purchase Truck Driver - Take Home $1,500+ weekly!
Western Express
location-iconBoston MA

CALL TO SPEAK WITH A SEATING SPECIALIST TODAY!(888) 981-4222Have you ever dreamed of owning your truck and being your own boss? Come experience the many reasons why Western Express is the best place to live out those dreams!This program was built for you to succeed, become an owner operator, and own your future.Western Express is now offering a wide variety of new and used trucks, so you can find the one that is right to call your own. With no money down, no credit check and no balloon payment, this walk-away lease is simply the best ownership program in the industry.***$2,500 SIGN-ON BONUS***We Offer:REAL RATES – Up to $2.00 per mile + industry-leading fuel surcharge on ALL MILES!GO BIG – $1,500/week median settlements AFTER expenses; Top Earners net $4,000+!GO HOME – No Forced Dispatch; Choose your Home Time!Great Selection of New and Used TrucksLow Weekly Payments (Between $575 - $745/week!)No Money Down, No Interest, No Balloon Payment, No Credit Check!Ownership in 3-5 years (depending on year/make/model selected)Business Tools and Guidance to help you manage and grow your businessAccess to some of the most inexpensive Insurance in the industryBig Discounts on Fuel and TiresBestPass to cover all Toll Expenses24/7 Operations and Maintenance Support$2,500 Sign-On Bonus!INTERESTED IN BEING A DRIVER TRAINER? Drive for us for 3 months or more and you can qualify as a driver trainer at Western Express! Call today for more details on how you can add up to 50% to your revenue!Have you been out of driving for 3 years or more? Are you a recent CDL-A grad? Call us for information about our Training Programs today!Requirements:Valid CDL-A (no experience required)21 Years of Age or OlderWestern Express is a non-discriminatory and equal opportunity employer. Regardless of background, we'd like to speak with you to see if you qualify.*Subject to change without notice. Some restrictions may apply. Call for details.

Full Time
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CDL-A Lease Purchase Truck Driver - Take Home $1,500+ weekly!
Western Express
location-iconBrookline MA

CALL TO SPEAK WITH A SEATING SPECIALIST TODAY!(888) 981-4222Have you ever dreamed of owning your truck and being your own boss? Come experience the many reasons why Western Express is the best place to live out those dreams!This program was built for you to succeed, become an owner operator, and own your future.Western Express is now offering a wide variety of new and used trucks, so you can find the one that is right to call your own. With no money down, no credit check and no balloon payment, this walk-away lease is simply the best ownership program in the industry.***$2,500 SIGN-ON BONUS***We Offer:REAL RATES – Up to $2.00 per mile + industry-leading fuel surcharge on ALL MILES!GO BIG – $1,500/week median settlements AFTER expenses; Top Earners net $4,000+!GO HOME – No Forced Dispatch; Choose your Home Time!Great Selection of New and Used TrucksLow Weekly Payments (Between $575 - $745/week!)No Money Down, No Interest, No Balloon Payment, No Credit Check!Ownership in 3-5 years (depending on year/make/model selected)Business Tools and Guidance to help you manage and grow your businessAccess to some of the most inexpensive Insurance in the industryBig Discounts on Fuel and TiresBestPass to cover all Toll Expenses24/7 Operations and Maintenance Support$2,500 Sign-On Bonus!INTERESTED IN BEING A DRIVER TRAINER? Drive for us for 3 months or more and you can qualify as a driver trainer at Western Express! Call today for more details on how you can add up to 50% to your revenue!Have you been out of driving for 3 years or more? Are you a recent CDL-A grad? Call us for information about our Training Programs today!Requirements:Valid CDL-A (no experience required)21 Years of Age or OlderWestern Express is a non-discriminatory and equal opportunity employer. Regardless of background, we'd like to speak with you to see if you qualify.*Subject to change without notice. Some restrictions may apply. Call for details.

Full Time
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Associate Scientist/Scientist I- Cell Engager (ODDU)
Takeda Pharmaceutical
location-iconBoston MA

By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice and Terms of Use. I further attest that all information I submit in my employment application is true to the best of my knowledge.Job DescriptionAbout the role:The Cell Engager team of the Oncology DDU is looking for an Associate Scientist/Scientist 1 with demonstrated in vivo/ex vivo skills in immuno-oncology drug discovery or translational sciences. You will be involved in discovery and development of novel therapeutics in the cell engager space, supporting new and ongoing pipeline programs using the COBRA and next generation immune engagers platform.This is a lab-based role. As an important member of the team, you will be responsible for new in vivo model development, target validation, assessing next-generation COBRA/immune cell engager concepts and advancing novel research molecules towards development candidates and IND. You will collaborate with important partners in the ODDU (IOI, C2H) GB, DSRE, DMPK, Translational teams and CTI.How you will contribute:Development and characterization of animal models to test the biological efficacy of therapeutic agents for oncology indications.Design in vivo efficacy models in xenograft and PDX models, ex vivo functional assays to assess therapeutic concepts aligned with principles of the COBRA platformLead or help with imaging studies to evaluate efficacy, biodistribution and mechanistic readouts using imaging modalities like PET/CT/IVIS platforms.Participate in analysis of in vivo studies to help establish PK/PD/efficacy relationships.Use immune readouts such FACS based immunophenotyping, cytokine profiling that can aid with both preclinical model selection and lead molecule screening.Familiar and help with ex vivo tissue profiling and sample collections for IHC, Nanostring analysis.Help with external collaborations with CROs and establish new protocolsExecute experiments and deliver comprehensive high quality data sets to help decision-makingIdentify state-of-the-art experimental protocols and IO in vivo modelsIdentify, plans, and executes well defined scientific projects and communicate program strategy and timelines to management.Present comprehensive technical or project reports and formal presentationsBe an in vivo lead on projects providing important scientific feedback to improve programs in a matrixed environment.Collaborate with others across sites and act as liaison for in vitro pharmacology and GB teams.Participate in and manage external interactions and collaborations with companies and academic research groups and potential collaboratorMinimum Requirements/Qualifications:Scientist 1: PhD in Immunology, Cell Biology or Biochemistry, or MS with 6+ years experience (industry experience preferred), or BS +8 years in Immunology, Cell Biology, Pharmacology.Associate Scientist: BS with at least 5 years of research experience or MS with at least 3 years of research in a lab setting working with animalsProficiency with in vivo efficacy rodent models, including mouse syngeneic, xenograft and PDX modelsExperimental skills, including mammalian tissue culture, in vivo model development, drug administration by multiple routes (IV, SQ, IP, IT, PO), and blood/tissue collection.Experience culturing and maintaining human tumor cell lines and primary human cells, preferably T cells and Macrophages, with best practices in tissue culture is important.Experience with ex vivo tumoroid/organoid cultures nice to have.Small animal In vivo imaging experience preferred across IVIS, PET/CT imaging modalities. Imaging data analysis knowledge across platformsKnowledge in immunology or immune oncology. Understanding of cell engagers and cell therapies.Experience with biologics (Antibodies, ADCs, Cell therapies etc.)Knowledge of protein biochemistry and experience conjugating the proteins with Fluorescent and radiolabeled probes.Hands –on basic experience with multi-color flow cytometry, molecular biology techniques (PCR, Gibson assembly, cloning etc), ELISA, MSD and other standard cell based, and non-cell based biochemical assays.Experience in molecular biology and biochemical techniques such as western blot, molecular cloning.Use of scientific databases and application for data management and data analysis (Graph Pad Prism, Soft Max Pro, Office 365, FlowJo etc).What Takeda can offer you:Comprehensive Healthcare: Medical, Dental, and VisionFinancial Planning & Stability: 401(k) with company match and Annual Retirement Contribution PlanHealth & Wellness programs including onsite flu shots and health screeningsGenerous time off for vacation and the option to purchase additional vacation daysCommunity Outreach Programs and company match of charitable contributionsFamily Planning SupportFlexible Work PathsTuition reimbursementMore about us:At Takeda, we are transforming patient care through the development of novel specialty pharmaceuticals and best in class patient support programs. Takeda is a patient-focused company that will inspire and empower you to grow through life-changing work.Certified as a Global Top Employer, Takeda offers stimulating careers, encourages innovation, and strives for excellence in everything we do. We foster an inclusive, collaborative workplace, in which our teams are united by an unwavering commitment to deliver Better Health and a Brighter Future to people around the world.In accordance with the CO Equal Pay Act, Colorado Applicants Are Not Permitted to Apply.EEO StatementTakeda is proud in its commitment to creating a diverse workforce and providing equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, gender expression, parental status, national origin, age, disability, citizenship status, genetic information or characteristics, marital status, status as a Vietnam era veteran, special disabled veteran, or other protected veteran in accordance with applicable federal, state and local laws, and any other characteristic protected by law.LocationsBoston, MAWorker TypeEmployeeWorker Sub-TypeRegularTime TypeFull time

Full Time
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CDL-A Lease Purchase Truck Driver - Take Home $1,500+ weekly!
Western Express
location-iconQuincy MA

CALL TO SPEAK WITH A SEATING SPECIALIST TODAY!(888) 981-4222Have you ever dreamed of owning your truck and being your own boss? Come experience the many reasons why Western Express is the best place to live out those dreams!This program was built for you to succeed, become an owner operator, and own your future.Western Express is now offering a wide variety of new and used trucks, so you can find the one that is right to call your own. With no money down, no credit check and no balloon payment, this walk-away lease is simply the best ownership program in the industry.***$2,500 SIGN-ON BONUS***We Offer:REAL RATES – Up to $2.00 per mile + industry-leading fuel surcharge on ALL MILES!GO BIG – $1,500/week median settlements AFTER expenses; Top Earners net $4,000+!GO HOME – No Forced Dispatch; Choose your Home Time!Great Selection of New and Used TrucksLow Weekly Payments (Between $575 - $745/week!)No Money Down, No Interest, No Balloon Payment, No Credit Check!Ownership in 3-5 years (depending on year/make/model selected)Business Tools and Guidance to help you manage and grow your businessAccess to some of the most inexpensive Insurance in the industryBig Discounts on Fuel and TiresBestPass to cover all Toll Expenses24/7 Operations and Maintenance Support$2,500 Sign-On Bonus!INTERESTED IN BEING A DRIVER TRAINER? Drive for us for 3 months or more and you can qualify as a driver trainer at Western Express! Call today for more details on how you can add up to 50% to your revenue!Have you been out of driving for 3 years or more? Are you a recent CDL-A grad? Call us for information about our Training Programs today!Requirements:Valid CDL-A (no experience required)21 Years of Age or OlderWestern Express is a non-discriminatory and equal opportunity employer. Regardless of background, we'd like to speak with you to see if you qualify.*Subject to change without notice. Some restrictions may apply. Call for details.

Full Time
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2022 GMU CMC Co-Op Purification Process Development
Sanofi
location-iconWaltham MA

Position Overview/Department Description The Genomic Medicine Unit (GMU) within Sanofi is responsible for the design and optimization of viral vector manufacturing processes and platforms. We chase the miracles of science through exploration of novel technologies to enable better characterization of our next-generation production platforms and to enable high-dose gene therapy programs. This 6-month position centers on viral vector purification processes but will interface with a broader team of vector and cell line engineering, upstream process development, analytics, and clinical manufacturing support.A successful candidate in this role will be engaged in actively learning new techniques, independently performing experiments, analyzing and presenting results, and collaborating with different functions to understand the cross-functional nature of decision-making. Experience in protein characterization, high-throughput, engineering and data analysis, analytical techniques, and/or viral vector purification is preferred. Project topic will be commensurate with level of previous experience.Key ResponsibilitiesDesign, execute, and analyze viral vector purification experiments.Perform analytical characterization of samples and analyze results.Work with cross-functional team for feedback and present findings.Contribute to technical reports and/or external publications if appropriate to project topic and level of experience.Basic QualificationsCurrently pursuing a Master's or Bachelor's study in biological sciences, genetic engineering/ engineering sciences with relevant study experience.Understanding of cell engineering, molecular biology, virology and immunology concepts.Knowledge and understanding of technologies and operations such as:Chromatography, tangential flow filtration, normal flow filtration, and/or viral clearance and inactivationAdvanced analytical tools to characterize protein and viral vectorsWork under minimal supervision and function within a collaborative, team-oriented environment.Ability to work in Biosafety Level 2, follow safe lab procedures, and maintain good laboratory practices (GLPs) including detail-oriented laboratory notebook documentation.Preferred QualificationsExperience with viral vector purification and characterization.Experience with SEC-HPLC, DLS, ddPCR/qPCR, Western blot, ELISA, FACS, immunoassays, spectroscopic and bioassay techniques.Experience with AKTA automated chromatography instruments, high-throughput liquid handlers, and automated filtration instruments.Experience with protein sequences and tools such as NanoSight 3000, Caliper LabChip GXII, Multi-Angle DLS (MADLS), ForteBio Octet, or similar instruments.Basic understanding of the principles of Quality by Design and ability to apply DOE to downstream development.Excellent communication skills and ability to build cross-functional relationships. At Sanofi R&D North America, we deliver meaningful solutions for patients. We transform science into breakthrough, best-in-class and first-in-class medicines and vaccines. We believe in creating a diverse and inclusive workforce - and workplace - which brings together the collective brainpower of over 2,000 colleagues and provides you with an exciting place to grow and develop. We set the bar high, and we deliver. Join us and together we will build on our trusted legacy of breakthroughs for society. Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law. As a healthcare company and a vaccine manufacturer, Sanofi has an important responsibility to protect individual and public health. All US based roles require individuals to be fully vaccinated against COVID-19 as part of your job responsibilities. According to the CDC, an individual is considered to be "fully vaccinated" fourteen (14) days after receiving (a) the second dose of the Moderna or Pfizer vaccine, or (b) the single dose of the J&J vaccine. Fully vaccinated, for new Sanofi employees, is to be fully vaccinated 14 DAYS PRIOR TO START DATE. PDNAt Sanofi diversity and inclusion is foundational to how we operate and embedded in our Core Values. We recognize to truly tap into the richness diversity brings we must lead with inclusion and have a workplace where those differences can thrive and be leveraged to empower the lives of our colleagues, patients and customers. We respect and celebrate the diversity of our people, their backgrounds and experiences and provide equal opportunity for all.

Full Time
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CDL-A Lease Purchase Truck Driver - Take Home $1,500+ weekly!
Western Express
location-iconWaltham MA

CALL TO SPEAK WITH A SEATING SPECIALIST TODAY!(888) 981-4222Have you ever dreamed of owning your truck and being your own boss? Come experience the many reasons why Western Express is the best place to live out those dreams!This program was built for you to succeed, become an owner operator, and own your future.Western Express is now offering a wide variety of new and used trucks, so you can find the one that is right to call your own. With no money down, no credit check and no balloon payment, this walk-away lease is simply the best ownership program in the industry.***$2,500 SIGN-ON BONUS***We Offer:REAL RATES – Up to $2.00 per mile + industry-leading fuel surcharge on ALL MILES!GO BIG – $1,500/week median settlements AFTER expenses; Top Earners net $4,000+!GO HOME – No Forced Dispatch; Choose your Home Time!Great Selection of New and Used TrucksLow Weekly Payments (Between $575 - $745/week!)No Money Down, No Interest, No Balloon Payment, No Credit Check!Ownership in 3-5 years (depending on year/make/model selected)Business Tools and Guidance to help you manage and grow your businessAccess to some of the most inexpensive Insurance in the industryBig Discounts on Fuel and TiresBestPass to cover all Toll Expenses24/7 Operations and Maintenance Support$2,500 Sign-On Bonus!INTERESTED IN BEING A DRIVER TRAINER? Drive for us for 3 months or more and you can qualify as a driver trainer at Western Express! Call today for more details on how you can add up to 50% to your revenue!Have you been out of driving for 3 years or more? Are you a recent CDL-A grad? Call us for information about our Training Programs today!Requirements:Valid CDL-A (no experience required)21 Years of Age or OlderWestern Express is a non-discriminatory and equal opportunity employer. Regardless of background, we'd like to speak with you to see if you qualify.*Subject to change without notice. Some restrictions may apply. Call for details.

Full Time
job-list-card-figure
Postdoctoral Fellow - Cardiovascular
Pfizer
location-iconCambridge MA

Why Patients Need YouPfizer s purpose is to deliver breakthroughs that change patients lives. Research and Development is at the heart of fulfilling Pfizer s purpose as we work to translate advanced science and technologies into the therapies and vaccines that matter most. Whether you are in the discovery sciences, ensuring drug safety and efficacy or supporting clinical trials, you will apply cutting edge design and process development capabilities to accelerate and bring the best in class medicines to patients around the world.What You Will AchieveWe are seeking a highly motivated postdoctoral fellow to join the cardiometabolism team within the Pfizer Internal Medicine Research Unit. The postdoc will work with Pfizer colleagues and mentors to uncover the mechanisms by which a novel protein regulates lipid trafficking. Under the guidance of research mentors, the successful candidate will drive the project forward with individual effort and independent study. The postdoc candidate should be independent and highly motivated with a keen interest in cardiometabolic disease and vascular cell biology.As a postdoctoral fellow, you will be at the center of our operations and you ll find that everything we do, every day, is in line with an unwavering commitment to quality. You will be part of the Research and Development team and will be responsible for conducting innovative science to drive new therapeutic discoveries. You will be relied on as a technical contributor to assess the assigned tasks and make decisions that involve direct application of your knowledge. It is your hard work and focus that will help in making Pfizer ready to achieve new milestones and help patients across the globe.How You Will Achieve ItDevelop and implement independent research ideas. Contribute intellectually and at the bench to the conception, design, execution, analysis, interpretation of data.Produce high quality data that will lead to first author publication(s) in high impact journals.Critically analyze experimental data, summarize and present results at internal and external meetings.Collaborate effectively with Pfizer colleagues in other disciplines.Ensure all tasks and responsibilities are performed according to scientific and ethical standards and correctly documented in lab notebook.Exercise and build basic team effectiveness skills e.g., commitment, feedback, consensus management) within context of immediate work group.QUALIFICATIONSMust-HaveRecent PhD (0-1 yrs) in biology, biochemistry, pharmacology or related field with demonstrated productivity in independent research (first author publication submitted/published in a high-quality peer-reviewed journal).Experience required in rodent (mouse) handling.Demonstrated proficiency in basic molecular and biochemical techniques required including some of the following: Cell culture, primary cell isolation, immunostaining, RNA/protein isolation from cells & tissues, qRT-PCR, Western blot, ELISA.Excellent written and oral communication skills.Well organized, self-motivated, team oriented, ability to multitask with attention to detailNice-to-HavePrevious training in vascular biology and/or lipid- related field is highly desired.PHYSICAL/MENTAL REQUIREMENTSAnimal handling requiredOTHER JOB DETAILSEligible for Relocation PackageEligible for Employee Referral BonusMust be authorized to work in the United States Pfizer requires all U.S. new hires to be fully vaccinated for COVID-19 prior to the first date of employment. As required by applicable law, Pfizer will consider requests for Reasonable Accommodations.Sunshine ActPfizer reports payments and other transfers of value to health care providers as required by federal and state transparency laws and implementing regulations. These laws and regulations require Pfizer to provide government agencies with information such as a health care provider s name, address and the type of payments or other value received, generally for public disclosure. Subject to further legal review and statutory or regulatory clarification, which Pfizer intends to pursue, reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act. Therefore, if you are a licensed physician who incurs recruiting expenses as a result of interviewing with Pfizer that we pay or reimburse, your name, address and the amount of payments made currently will be reported to the government. If you have questions regarding this matter, please do not hesitate to contact your Talent Acquisition representative.EEO & Employment EligibilityPfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status. Pfizer also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA. Pfizer is an E-Verify employer.Research and Development

Full Time
job-detail-figure
Academic Abdominal Radiologist - Tufts Medical Center - Boston, MA
share-icon
Full Time
location-iconBoston MA
Job Description
Description:

The Department of Radiology at Tufts Medical Center is seeking a 1.0FTE Academic Abdominal Radiologist for a full-time faculty appointment at the rank of Assistant, Associate, or Professor at Tufts University School of Medicine.

Why join our team:

The Abdominal Imaging Division is a collaborative and inclusive team that interprets abdominal/pelvic radiography, fluoroscopy, ultrasound, CT, and MRI; and there is dedicated academic time and formal mentorship of radiologists that is championed by the Chair who supports the academic mission of excellence in teaching and clinical, translational research.

We are a subspecialized academic radiology department with a diverse practice, and we have acquired within the past year 8 new GE ultrasounds, the most advanced CT Siemens scanner, and are acquiring 2 new 3.0T and a 1.5T MRI which will be equipped with the most advanced body MR sequences and the most cutting edge post processing techniques like compressed sensing with deep learning (AI) reconstruction techniques. There will be novel multiparametric prostate MR imaging and advanced liver imaging including elastography, fat quantification and iron quantification.

How you will transform patient care:

  • You will have a faculty appointment at Tufts University School of Medicine.
  • You will work with over 20 diagnostic radiology residents and a dedicated body MR fellow.
  • You will join a team of faculty members who are actively engaged in resident and medical student education including teaching conferences, multidisciplinary conferences, and research projects.
  • You will have ample chances to contribute to a team culture that is dedicated to inclusivity, collaboration, innovation, and work life balance.
  • You will have access to the Tufts Clinical and Translational Science Institute to support research initiatives that includes collaborations in Artificial Intelligence with Massachusetts Institute of Technology (MIT) and formal mentorship in grant applications from successfully funded researchers across the medical school faculty.
  • You will have access to New 3.0T MR is being installed this fall with highest gradients, compressed sensing with deep learning (DL) technology, and access to a clinical MR support scientists for works in progress, and an additional 1.5T and 3.0T MR. There are 3 Siemens scanners: two 192 slice dual energy and one, 64 slice with an interventional package, and 8 newly purchased ultrasound machines.

Who you are:

  • Completed a Body Imaging Fellowship and be ABR or AOBR certified or eligible.
  • Expertise in CT, MRI, and ultrasound imaging.
  • Knowledge of advanced body MR techniques and spectral CT is a plus.
  • A team player who works cooperatively with a wide range of stakeholders and disciplines that fosters excellence in patient care and enhances patient experience.
  • A radiologist who enjoys teaching residents and supports academic projects/research and who wants to work in an academic environment.

COVID-19 Policy:

To protect patients, physicians, staff, visitors, and the community from the COVID-19 infection, vaccination for COVID-19 is mandatory for employment unless an exemption is granted for medical or religious reasons.

Work, Live, and Grow:

Boston, Massachusetts is a dynamic, innovative, and historic city with something for everyone. Whether you seek cultural attractions, an intellectual environment, music and entertainment, museums, night life, shopping, fitness, food festivals, or a sunset harbor cruise- you will find it here. The city of Boston is ideally located in close proximity to the coastal beach towns of Cape Cod and the Berkshires in Western Massachusetts, the White Mountains of New Hampshire, and the Green Mountains of Vermont which offer great summertime recreational activities from swimming, sailing, fishing, hiking, and rock climbing and great winter activities from Nordic skiing to downhill skiing and snowboarding. Boston consistently ranks as one of the most desirable places in the country to live and to raise a family.

We pride ourselves on having an inclusive work environment for all of our employees. We offer very competitive salaries and benefits packages including health, dental, and vision insurance and retirement plans.

Location: Tufts Medical Center in downtown Boston, Massachusetts.

How to apply:

You can submit an application via the apply button located at the top of the listing.

Should you have any questions regarding the position or any complications submitting an application with us, please feel free to reach out to Ryan Scerra, Senior Provider Recruiter, at ryan.scerra@wellforce.org.

Why Wellforce:

Tufts Medical Center is a proud member of Wellforce. Wellforce brings together providers and organizations with a shared vision of high-quality care delivered in the setting that serves our patients best. Together, Wellforce brings together the strength of both academic medicine and community care.

Diversity, Equity, Inclusion, and Social Responsibility: We truly believe our employees' diverse backgrounds, experiences, and perspectives are a powerful contributor to creative an inclusive environment where everyone can thrive and reach their maximum potential while adding value to both our organization and our patients. We warmly welcome all candidates of diverse origin, background, ability, age, sexual orientation, gender identity, and personality.

.Requirements:

PI155842323

job-detail-figure
Academic Abdominal Radiologist - Tufts Medical Center - Boston, MA
share-icon
Full Time
location-iconBoston MA
Job Description
Description:

The Department of Radiology at Tufts Medical Center is seeking a 1.0FTE Academic Abdominal Radiologist for a full-time faculty appointment at the rank of Assistant, Associate, or Professor at Tufts University School of Medicine.

Why join our team:

The Abdominal Imaging Division is a collaborative and inclusive team that interprets abdominal/pelvic radiography, fluoroscopy, ultrasound, CT, and MRI; and there is dedicated academic time and formal mentorship of radiologists that is championed by the Chair who supports the academic mission of excellence in teaching and clinical, translational research.

We are a subspecialized academic radiology department with a diverse practice, and we have acquired within the past year 8 new GE ultrasounds, the most advanced CT Siemens scanner, and are acquiring 2 new 3.0T and a 1.5T MRI which will be equipped with the most advanced body MR sequences and the most cutting edge post processing techniques like compressed sensing with deep learning (AI) reconstruction techniques. There will be novel multiparametric prostate MR imaging and advanced liver imaging including elastography, fat quantification and iron quantification.

How you will transform patient care:

  • You will have a faculty appointment at Tufts University School of Medicine.
  • You will work with over 20 diagnostic radiology residents and a dedicated body MR fellow.
  • You will join a team of faculty members who are actively engaged in resident and medical student education including teaching conferences, multidisciplinary conferences, and research projects.
  • You will have ample chances to contribute to a team culture that is dedicated to inclusivity, collaboration, innovation, and work life balance.
  • You will have access to the Tufts Clinical and Translational Science Institute to support research initiatives that includes collaborations in Artificial Intelligence with Massachusetts Institute of Technology (MIT) and formal mentorship in grant applications from successfully funded researchers across the medical school faculty.
  • You will have access to New 3.0T MR is being installed this fall with highest gradients, compressed sensing with deep learning (DL) technology, and access to a clinical MR support scientists for works in progress, and an additional 1.5T and 3.0T MR. There are 3 Siemens scanners: two 192 slice dual energy and one, 64 slice with an interventional package, and 8 newly purchased ultrasound machines.

Who you are:

  • Completed a Body Imaging Fellowship and be ABR or AOBR certified or eligible.
  • Expertise in CT, MRI, and ultrasound imaging.
  • Knowledge of advanced body MR techniques and spectral CT is a plus.
  • A team player who works cooperatively with a wide range of stakeholders and disciplines that fosters excellence in patient care and enhances patient experience.
  • A radiologist who enjoys teaching residents and supports academic projects/research and who wants to work in an academic environment.

COVID-19 Policy:

To protect patients, physicians, staff, visitors, and the community from the COVID-19 infection, vaccination for COVID-19 is mandatory for employment unless an exemption is granted for medical or religious reasons.

Work, Live, and Grow:

Boston, Massachusetts is a dynamic, innovative, and historic city with something for everyone. Whether you seek cultural attractions, an intellectual environment, music and entertainment, museums, night life, shopping, fitness, food festivals, or a sunset harbor cruise- you will find it here. The city of Boston is ideally located in close proximity to the coastal beach towns of Cape Cod and the Berkshires in Western Massachusetts, the White Mountains of New Hampshire, and the Green Mountains of Vermont which offer great summertime recreational activities from swimming, sailing, fishing, hiking, and rock climbing and great winter activities from Nordic skiing to downhill skiing and snowboarding. Boston consistently ranks as one of the most desirable places in the country to live and to raise a family.

We pride ourselves on having an inclusive work environment for all of our employees. We offer very competitive salaries and benefits packages including health, dental, and vision insurance and retirement plans.

Location: Tufts Medical Center in downtown Boston, Massachusetts.

How to apply:

You can submit an application via the apply button located at the top of the listing.

Should you have any questions regarding the position or any complications submitting an application with us, please feel free to reach out to Ryan Scerra, Senior Provider Recruiter, at ryan.scerra@wellforce.org.

Why Wellforce:

Tufts Medical Center is a proud member of Wellforce. Wellforce brings together providers and organizations with a shared vision of high-quality care delivered in the setting that serves our patients best. Together, Wellforce brings together the strength of both academic medicine and community care.

Diversity, Equity, Inclusion, and Social Responsibility: We truly believe our employees' diverse backgrounds, experiences, and perspectives are a powerful contributor to creative an inclusive environment where everyone can thrive and reach their maximum potential while adding value to both our organization and our patients. We warmly welcome all candidates of diverse origin, background, ability, age, sexual orientation, gender identity, and personality.

.Requirements:

PI155842323