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Clinical Reimbursement Specialist
Next Step Healthcare
location-iconWoburn MA

Next Step Healthcare is seeking an experienced Clinical Reimbursement Specialist to support our MDS/MMQ teams in Massachusetts.The Clinical Reimbursement Specialist provides extensive training, analysis, advice and consultation to the facilities and teams within his/her area of responsibility. Ensures compliance with federal and state regulations, as well as Company policy and procedures regarding state case mix/Medicare and Managed Care payment systems. Monitors, consults, and makes effective recommendations for changes and modifications to existing facility processes, systems, policies, and practices which will assure efficient, effective and compliant state Medicaid/Medicare/Managed Care payment performance.Full-time; home office based position with 3-4 travel days per week covering North Boston, Central & Western MA.Job Functions include but are not limited to:Provides consultation, training and support concerning the Medicare, Managed Care and state case mix payment system for the assigned area.Analyzes systems and processes to determine that federal and state regulations as well as company policies and procedures are followed. Promotes compliance by performing periodic audits of MDS assessments, supporting documentation, and other relevant data.Recognizes, advises and promotes facility best practices and systems for dealing with state case mix/Medicare and Managed Care payment systems.Studies, analyze and reports period over period information and systems in order to identify trends and deviations from results in Medicare, Managed Care and State Case Mix Index and takes appropriate actions.Works in conjunction with teams to resolve issues effecting deviations from expected results. Recommends changes and performs follow-up to ensure that those recommendations are effectively implemented and monitored for appropriateness.Regularly communicates to management outside the facility on recommendations made to facility management to ensure proper implementation and follow-up.Serves as a liaison between state and organization related to the state case-mix process, including electronic submission and state MDS requirements related to state payment.Assists in the recruitment/interview process for MDS and MMQ vacancies.Qualifications:Licensed as a Registered Nurse in the State of MassachusettsThree to Five years of clinical experience in a long-term care setting, which includes supervisory, administrative or consultative capacities.Current knowledge of computer technology and systems.Ability to work independently with minimal supervision and guidance.Extensive knowledge of MDS and back-up documentation required and extensive knowledge of state grouper and calculator field relative to MDS and state payment.Extensive knowledge of Medicare reimbursement, RUG IV system, compliance and eligibility.Must be willing and able to travel extensively and maintain a valid driver’s license.We offer competitive compensation and benefit plans including:Vacation, sick and holiday payMedical, Dental, Vision InsuranceST/LT Disability InsuranceTuition ReimbursementLife Insurance401KAt Next Step Healthcare, we know that working in the healthcare industry is more than just a job – it’s a way of life reserved for the most compassionate, caring, and hard-working individuals. Are you ready to take the next step in your career? Apply today.Next Step Healthcare is an equal opportunity employer. We embrace diversity and are committed to fostering an inclusive workplace for all employees.HPIND1233vMm8GDLEA

Part Time / Full Time
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Senior Research Associate II, Protein Purification, Global Biologics
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 Description About the role: At Takeda, we are a forward-looking, world-class R&D organization that unlocks innovation and delivers transformative therapies to patients. By focusing R&D efforts on four therapeutic areas and other targeted investments, we push the boundaries of what is possible in order to bring life-changing therapies to patients worldwide. Join Takeda as a Senior Research Associate II where you will be apart of the protein purification team. You will be responsible for the purification and biotinylation of recombinant proteins and antibodies to supply the reagents and therapeutic candidates in drug discovery and development research. As part of the Therapeutic Generation and Screening Team, you will report to the Senior Scientist and work with the Global Biologics organization. How you will contribute: Independently develop and implement protein purification and protein conjugation strategies to support drug development projects and technology development programs.Execute protein purification with affinity, size exclusion, and ion exchange chromatography using AKTA systems.Perform protein analysis and characterization including SDS-PAGE, HPLC, and western blot.Perform protein labeling (e.g. bioinylation) to generate the reagents for biologics discovery campaigns and analysis.Troubleshoot protein purification and conjugation methods.Follow appropriate procedures to record data in the internal databases and electronic lab notebooks.Design and execute various purification methods to purify proteins from medium to large-scale shake flasks or wave bags culture.Communicate research and development findings with internal and external partners.Use literature to increase knowledge base and implement improvements. Minimum Requirements/Qualifications: BS in Biochemistry or related discipline with 4+ years relevant experience, or MS in Biochemistry or related discipline, with 2+ years relevant experience.Demonstrated experience in protein purification (with an AKTA FPLC system).Demonstrated experience with software used for data presentation and communications.Demonstrated experience working on project teams to develop protein-based therapeutics.Experience with protein database entry such as gene data biologics.Demonstrated experience with conjugation chemistries; NHS based conjugation is desirable.Capable to work independently to solve scientific questions. 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 reimbursement More 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 Statement Takeda 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, MA Worker TypeEmployee Worker Sub-TypeRegular Time TypeFull time

Part Time / Full Time
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Scientist I/II, Investigative Toxicology
Takeda Pharmaceutical
location-iconCambridge 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 Description About the role: The Global Investigative Toxicology team is a cross-functional team of scientists that aim to detect and de-risk toxicity in Takeda's portfolio to help make medicines safer and more effective. We are looking for a Research Scientist to support these efforts across platforms and modalities. The Research Scientist will contribute ideas and deliver decision-making data to inform project teams on improved efficacy and/or de-risking of potential toxicities.Work as part of a global team of safety assessment scientists to detect and de-risk toxicities associated Takeda assets.Design and implement early safety assessment screening strategies to enable the progression of optimized therapeutic candidates.Conduct cell-based in vitro assays to characterize toxicities for medicines in discovery & development.Develop novel in vitro model systems to assess safety risks associated Takeda assets. Join Takeda as a Scientist I/II, Investigative Toxicology , based in Cambridge, MA. How you will contribute: ACCOUNTABILITIES Develop, design, execute, and interpret in vitro cell-based assays to characterize diverse mechanisms of toxicity with a focus on rare disease and gene therapy therapeutics.Maintain cultures of immortalized cancer cell lines, primary cell types of various origin (lung, liver, kidney, intestine, pancreas, blood etc.).Prepare experimental protocols, analyze experimental data, and present study results in team and department meetings.Contribute ideas to drive innovation within investigative toxicology and with key collaborators (e.g. pharmacology, DMPK, bioinformatics).Good documentation practices are required. Minimum Requirements/Qualifications:Ph.D. with 0-2 years or MS with 6+ years or BS with 8+ years of experience in biology, biochemistry, pharmacology, or a related discipline.Expert with standard aseptic cell culture technique, including experience culturing various cell types. Experience with culturing and differentiating primary cells is a plus.Broad experience with cell-based functional assays. Experience with cell transfection/transduction, imaging, and flow cytometry is a plus.Basic experience with molecular biology techniques including RNA/DNA extraction, qPCR, and western blot.Experience working in a matrixed team environment at a pharmaceutical company and/or CRO.Broad scientific knowledge in hematology, immunology, and pharmacology.Self-motivated with strong time management and organizational skills.Ability to balance multiple projects and flexible with changing priorities.Highly collaborative with demonstrated ability to work in a matrixed team environment.Excellent oral and written communication skills. 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 reimbursement More 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 Statement Takeda 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. LocationsUSA - MA - Kendall Square Worker TypeEmployee Worker Sub-TypeRegular Time TypeFull time

Part Time / Full Time
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Research Associate Scientist I- In vivo- Oncology Drug Discovery Unit
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 Description About the role: The Oncology Drug Discovery Unit (ODDU) is looking for an Associate Scientist to join a collaborative and dynamic team. You will oversee the discovery and development of novel therapeutics supporting new and ongoing pipeline programs in the ODDU. This is a lab-based role and you will work with the in vivo lead and and be responsible for critical path activities with demonstrated in vivo skills in immuno-oncology drug discovery or translational sciences. You should have a foundation in in vivo models specifically related in vivo and ex vivo pre-clinical models of cancer. As an important member of the team, you will be responsible for new model development, cell line characterization, target validation, assessing therapeutic concepts of several immune engager molecules and advancing development candidates to IND. You will collaborate with important partners, including those in the ODDU and those in partnering organizations (Global Biologics, DSRE, DMPK, and Translational Oncology). How you will contribute: Develop animal models to test the biological efficacy of therapeutic agents for oncology indicationsDesign and implement in vivo efficacy models in xenograft and PDX modelsParticipate in analysis of in vivo studies to help establish PK / PD / efficacy relationships.Help with external collaborations with CROs and and establish new protocolsExecute experiments with minimal supervision and deliver comprehensive high quality data sets to help decision-makingIdentify experimental protocols and in vivo modelsIdentify, plan, and execute well defined scientific projects and communicates program strategy and timelines to management.Interpret results of complex experimentsPrepare and present comprehensive technical or project reports and formal presentationsMaintain laboratory notebooks and follow laboratory practices in compliance Minimum Requirements/Qualifications: MS in a scientific discipline (or equivalent) with 3+ years relevant industry experience, or BS in a scientific discipline with 5+ years experience, or Associates degree in scientific discipline with 7+ years relevant industry experienceProficiency 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. Imaging experience is highly desirable.Experience culturing and maintaining human tumor cell lines and primary human cells, preferably T cells, with best practices in tissue culture is important.Knowledge in immunology or immune oncology. Understanding of cell and gene therapies.Experience with biologics is prefered (Antibodies, ADCs, Cell therapeis etc)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 is a plus.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 reimbursement More 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 field-based employees must be fully vaccinated for COVID-19, as a condition of employment. Base Salary Range: $ 87,500 to $ 125,000. Employees may also be eligible for Short Term and Long-Term Incentive benefits. Employees are eligible to participate in Medical, Dental, Vision, Life Insurance, 401(k), Charitable Contribution Match, Holidays, Personal Days & Vacation, Tuition Reimbursement Program and Paid Volunteer Time Off. The final salary offered for this position may take into account a number of factors including, but not limited to, location, skills, education, and experience. EEO Statement Takeda 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, MA Worker TypeEmployee Worker Sub-TypeRegular Time TypeFull time

Part Time / Full Time
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Senior Research Associate II / Research Associate Scientist, Cell Therapy Innovation
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 Description About the role: At Takeda, we are a forward-looking, world-class R&D organization that unlocks innovation and delivers transformative therapies to patients. By focusing R&D efforts on four therapeutic areas and other targeted investments, we push the boundaries of what is possible in order to bring life-changing therapies to patients worldwide. Join Takeda as a Senior Research Associate II / Associate Scientist where you will play an integral role in charging of multiple scale viral vector production and QC assay, as well as lead/participate in technology development to support pre-clinical research as part of a larger multi-disciplinary team effort. As part of the Viral Vector Innovation team of Takeda Cell Therapy Innovation team you will report to the Lead, Novel Technologies, Cell Therapy Innovation. How you will contribute: Participate and lead projects to enable high throughput automation operation of viral vector production and QC testing. Join a collaborative effort to establish automated data processing, and prediction models. Design and execute experiments independently with a focus on improving vector design, production process, as well as deepen the knowledge of retroviral vector biology. Review, communicate data internally (e.g., to supervisor, project teams) and prepares technical reports. Proposes and implements resolutions to solve technical problems Assists with the development of project strategy and communicates complex data/decisions within department and cross functionally as necessary. Keep accurate and complete documentation of experimental studies in the ELN and contribute to technical reports and protocols. Work with BSL 2 materials, follow safe lab procedures and maintain good laboratory practices (GLPs). Stay updated on new, relevant technologies and published literature to support innovation within the group. Lead new technology evaluations to increase product yield and process understanding. Occasionally, perform weekend and holiday work to support on-going lab activities. Work with senior team leaders and cross-functional teams and provide scientific and technical recommendations. Minimum Requirements/Qualifications: Research Associate Scientist: MS with 3+ years relevant experience, or BS with 5+ years relevant experience with degrees in biology, biotechnology, molecular biology, biomedical engineering or related pharmaceutical sciences. Senior Research Associate II: MS with 2+ years relevant experience, or BS with 4+ years relevant experience with degrees in biology, biotechnology, molecular biology, biomedical engineering or related pharmaceutical sciences. Experience with or practical knowledge about statistical software, data science, automation, database, machine learning and artificial intelligence is preferred. Previous experience with molecular and cell biology, transfection, viral vector engineering, production, and purification. Experience with adherent and/or suspension cell culture techniques with strong understanding of aseptic operations is required. Hands-on experience with a range of analytical techniques, such as infectious titer assay, microscopy, flow cytometry, PCR, ELISA, western blotting, immunofluorescent staining and image analysis are required. Experience with the automated liquid handler and/or high-throughput processes is a plus. Experience working in a multi-disciplinary team environment. What Takeda can offer you: Comprehensive Healthcare: Medical, Dental, and Vision Financial Planning & Stability: 401(k) with company match and Annual Retirement Contribution Plan Health & Wellness programs including onsite flu shots and health screenings Generous time off for vacation and the option to purchase additional vacation days Community Outreach Programs and company match of charitable contributions Family Planning Support Flexible Work Paths Tuition reimbursement More 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 Statement Takeda 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, MA Worker TypeEmployee Worker Sub-TypeRegular Time TypeFull time

Part Time / Full Time
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Research Associate Scientist / Research Scientist I, Cell Therapy Innovation
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 Description About the role: At Takeda, we are a forward-looking, world-class R&D organization that unlocks innovation and delivers transformative therapies to patients. By focusing R&D efforts on four therapeutic areas and other targeted investments, we push the boundaries of what is possible in order to bring life-changing therapies to patients worldwide. Join Takeda as a Research Associate Scientist / Research Scientist I where you will play an integral role in charging of multiple scale viral vector production and QC assay, and lead/participate in technology development to support pre-clinical research as part of a larger multi-disciplinary team effort. As part of the Viral Vector Innovation team of Takeda Cell Therapy Innovation you will report to the Lead, Novel Technologies, Cell Therapy Innovation. How you will contribute: Design and execute experiments independently with a focus on improving vector design, production process, and deepen the knowledge of retroviral vector biology. Review, interpret and communicate data internally (e.g., to supervisor, project teams) and prepares technical reports. Propose and implement resolutions to solve technical problems Help develop project strategy and communicate complex data/decisions within department and cross functionally Keep accurate and complete documentation of experimental studies in the ELN and contribute to technical reports and protocols. Work with BSL 2 materials, follow safe lab procedures and maintain good laboratory practices (GLPs). Stay updated on new, relevant technologies and published literature to support innovation within the group. Lead new technology evaluations to increase product yield and process understanding. Occasionally, perform weekend and holiday work to support ongoing lab activities. Work with senior team leaders and cross-functional teams and provide scientific and technical recommendations. Minimum Requirements/Qualifications: Research Scientist I: PhD with 0+, or MS with 6+ years relevant experience, or BS with 8+ years relevant experience with degrees in biology, biotechnology, molecular biology, biomedical engineering or related pharmaceutical sciences. Research Associate Scientist: MS with 3+ years relevant experience, or BS with 5+ years relevant experience with degrees in biology, biotechnology, molecular biology, biomedical engineering or related pharmaceutical sciences. Previous experience with molecular and cell biology, transfection, viral vector engineering, production and purification. Experience with adherent and/or suspension cell culture techniques with strong understanding of aseptic operations is required. Hands-on experience with a range of analytical techniques, such as but not limited to infectious titer assay, microscopy, flow cytometry, PCR, ELISA, western blotting, immunofluorescent staining and image analysis are required. Experience with automated liquid handler and/or high-throughput processes is a plus. Experience with or practical knowledge about statistical software, data science, automation, database, machine learning and artificial intelligence is preferred. Experience in working in a multi-disciplinary team environment. What Takeda can offer you: Comprehensive Healthcare: Medical, Dental, and Vision Financial Planning & Stability: 401(k) with company match and Annual Retirement Contribution Plan Health & Wellness programs including onsite flu shots and health screenings Generous time off for vacation and the option to purchase additional vacation days Community Outreach Programs and company match of charitable contributions Family Planning Support Flexible Work Paths Tuition reimbursement More 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 Statement Takeda 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, MA Worker TypeEmployee Worker Sub-TypeRegular Time TypeFull time

Part Time / Full Time
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Bioanalytical Scientist
Pharmaron
location-iconWoburn MA

Job DescriptionPharmaron (Boston) Lab Services LLC, 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!Pharmaron Lab Services 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.Pharmaron Lab Services is proud to be an Equal Employment Opportunity and Affirmative Action employer.

Part Time / Full Time
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Class A CDL Truck Driver LEASE PURCHASE - Take Home $1,500+ weekly!
Western Express
location-iconSalem 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.

Part Time / Full Time
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Research Associate I
Cystic Fibrosis Foundation
location-iconLexington MA

The Cystic Fibrosis Foundation is a leading healthcare nonprofit organization like no other. For decades, we have been taking major steps and pioneering new ways to advance the mission to find a cure for cystic fibrosis and to provide all people with CF the opportunity to lead long, fulfilling lives by funding research and drug development, partnering with the CF community, and advancing high-quality, specialized care. We are the global leader in the search for a cure for cystic fibrosis and nearly every CF drug and therapy available today was made possible because of CF Foundation support. We did this not only for the close to 40,000 people living in the U.S. with CF and the estimated 105,000 people worldwide but for the people with CF and families who have worked tirelessly to support the mission. These achievements have required dedication and unwavering commitment from a talented team of CF Foundation employees. We promote an environment that attracts and retains a diverse group of talented people who are passionate about eradicating this disease . Join us and you will join an amazing team, devoted to our community, and our mission. Position Description The Cystic Fibrosis Foundation (CF Foundation) and its employees embrace their commitment to its core values. These core values are the pillars on which the CF Foundation stand and will continue to sustain us as we move forward. Keep sight of what really matters: Our decisions are based on what is best for people with cystic fibrosis and their families. Aspire for excellence in all we do: We take pride in our work. We are committed to continuous learning and improvement. Stronger together: We collaborate and work together so that we can learn more and achieve more. Innovate with courage: We embrace challenges. We reach beyond boundaries in pursuit of our vision. Care about our people: We deeply care about each other and all who support our shared mission. We listen with respect. We support one another. We are a nonprofit, donor-supported organization that has raised and invested billions of dollars to help develop cystic fibrosis therapies that have changed the lives of people with this disease. Nearly every CF medicine available today was made possible because of Foundation support. POSITION SUMMARY: The Research Associate I will conduct laboratory functions under direct supervision of the supervisor. They will work in compliance with established protocols, procedures, and regulatory requirements to achieve departmental goals. ESSENTIAL DUTIES AND RESPONSIBILITIES: Perform day-to-day experimental activities including human material procurement activities i.e., preservation, sterility, handling, and preparing for distribution of cell material. Become proficient in the use of Ion transport/electrophysiological assays and assist in assay design. Prepare, cultivate, QC (including Ion Transport assays), and bank primary cells from lung tissue, nasal scrapings, and rectal biopsies. Perform standard lab techniques such as tissue culture, transfections, test article dilutions, make media/buffers, perform Western blots, tissue fixation etc. with some supervision. Will keep accurate records, and present data, may help in preparation of external communications (i.e., posters). Performs laboratory experiments using standard techniques and equipment. Performs troubleshooting and quality control of experimental activities. Performs related lab maintenance such as maintaining and cleaning equipment and ordering supplies. Performs calculations to complete research test results; collates data; and performs analysis of lab results for discussion with supervisor. Collates results in preparation for internal meetings. Participates in group meetings for discussion of data and suggested next steps. Maintains detailed records of the work conducted (electronic lab notebook). Prepares and presents results at internal meetings. KNOWLEDGE, SKILLS, AND ABILITIES REQUIRED: B.S. in Life Sciences with 0-2 years R+D laboratory experience. Excellent attention to detail. Excellent communication, collaboration, problem solving skills. Detail-oriented and capable of multi-tasking in a dynamic team. REPORTING RELATIONSHIPS: Reports to the Research Scientist I. No direct reports. WORKING CONDITIONS: Commute to lab every workday. Research Lab with chemical and biological hazards present. Must have access to reliable transportation. Use of computer required. Must be able to work from home when road conditions do not permit travel to workplace. Sitting, bending, reaching, and walking. The above is intended to describe the general content of and requirements for the performance of this job. It is not to be construed as an exhaustive statement of essential functions, responsibilities, or requirements. Total Rewards: The CF Foundation is committed to offering competitive compensation (base pay and incentive), benefits, and professional development opportunities that maximize our ability to recruit, retain, reward, and motivate a highly-qualified and diverse workforce. Our comprehensive benefits package includes medical, dental, and vision coverage; generous time-off and leave policies; a holistic well-being program; health savings and flexible spending accounts; employer-provided life and disability insurance; retirement savings benefits; and a variety of work-life benefits to support employees and their family members. The CF Foundation is an equal opportunity employer that is committed to being an employer of choice, not just a good place to work, but a great and inclusive place to work. We strive to recruit and maintain a diverse workforce. Qualified applicants will receive consideration for employment without regard to race, physical or mental disability, color, religious creed, ancestry, national origin, religion, age, sex, marital status, genetic information or testing, gender identity and expression, sexual orientation or status as a Vietnam-era or special disabled veteran or any characteristic protected by law. Reasonable Accommodations: The CF Foundation is committed to providing reasonable accommodations for qualified individuals with disabilities in our job application procedures. If you need assistance or would like to request an accommodation due to a disability, please contact us at .

Part Time / Full Time
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Experienced Construction Superintendent - Boston, MA
AECOM
location-iconBoston MA

Job DescriptionCompany DescriptionAt AECOM, we’re delivering a better world. We believe infrastructure creates opportunity for everyone. Whether it’s improving your commute, keeping the lights on, providing access to clean water or transforming skylines, our work helps people and communities thrive.Our clients trust us to bring together the best people, ideas, technical expertise and digital solutions to our work in transportation, buildings, water, the environment and new energy. We’re one global team – 47,000 strong – driven by a common purpose to deliver a better world. About Construction Management - AECOM TishmanSince 1898, AECOM Tishman has managed the construction of some of the world’s most iconic buildings. We employ a diversified preconstruction and construction management staff of structural, mechanical, electrical, and civil engineers; architects; technology specialists; scheduling and cost control personnel; and construction estimators and accountants. We provide expert consultation and guidance in all phases of a building project, from master-planning, preconstruction options evaluation and decision-making, to design review, estimating, and scheduling, through procurement, construction and occupancy. AECOM Tishman’s staff manages all consultants and contractors on a project, representing client interests throughout the project cycle. In total, AECOM Tishman has built more than 900 million square feet – including the tallest building in the Western Hemisphere, One World Trade Center in New York.Job DescriptionAECOM Tishman is seeking an experienced an experienced Construction Superintendent to support our iconic building projects in Boston, MA.Job Description:Provide overall on-site administrative and technical management for a wide range of construction projects.       Responsible for the organization and direction of construction and related activities within assigned area of responsibility, which may be a single area, multi-area or a multi-discipline construction project.May be the primary client contact for all jobsite day to day activities, or may coordinate with client’s resident representatives on jobsite activities within assigned area of operations.Responsibilities are to ensure assigned jobsite operations are in compliance with design/specifications, completion on schedule, within budget and to quality standards.Interfaces with all other administrative field staff, field management staff and particularly the Project Manager in a coordinated effort.Job Summary: The construction superintendent is responsible to lead and manage the on-site construction team and oversee all work on site. The construction superintendent will be responsible for orderliness on-site and ensure compliance with safety regulations. They will ensure quality standards are met, and all equipment and materials are available on-site at all times. They will liaise with inspection authorities regarding approvals.To ensure success you should complete projects on time and within budget, and not compromise on quality. Top candidates will be strong leaders, pro-active, and perform well under pressure.Construction Superintendent Responsibilities:Leading and managing the on-site construction team.Coordinating and overseeing all work on site.Attending project meetings.Reviewing and becoming familiar with the schedule and budget and ensuring adherence to these.Ensuring quality standards are met.Following the project timeline to ensure deadlines are met.Monitoring and ensuring on-site safety compliance, cleanliness, and orderliness.Maintaining records for site personnel such as daily field reports, field orders, and RFIs.Liaising with inspection authorities regarding approvals.QualificationsMinimum Requirements:BS Civil Engineering/Constuction Management and 6 years of Construction Superintendent experience or AA/AS and 8 years of relevant construction experience or HSD/GED and 10 years of relevant construction experience, or demonstrated equivalency of experience and/or education.Preferred Qualifications:5 years of experience as a Superintendent for a large general contractor.Experience in the field of life sciences or campus construction.Experience in managing teams.Experience in the oversight and management of subcontractors.Experience in vertical construction.OSHA 30Experience in the development of a culture of safety.Experience with ProcoreProficiency in Microsoft Office Suite (Word, Excel, Outlook, Teams)Experience in ensuring construction jobsite is compliant with all specifications, budgets and quality standards. Additional InformationThis position does not include sponsorship for United States work authorization.This position may include relocation benefits.All your information will be kept confidential according to EEO guidelines.With infrastructure investment accelerating worldwide, our services are in great demand, and there’s never been a better time to be at AECOM! Join us, and you’ll get all the benefits of being a part of a global, publicly traded firm – access to industry-leading technology and thinking and transformational work with big impact and work flexibility.AECOM provides a wide array of compensation and benefits programs to meet the diverse needs of our employees and their families. We also provide a robust global well-being program. We’re the world’s trusted global infrastructure firm, and we’re in this together – your growth and success are ours too.As an Equal Opportunity Employer, we believe in each person’s potential, and we’ll help you reach yours.Join us and let’s get started.

Part Time / Full Time
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Immediate need - Construction Project Engineer
AECOM
location-iconBoston MA

Job DescriptionCompany DescriptionAt AECOM, we’re delivering a better world. We believe infrastructure creates opportunity for everyone. Whether it’s improving your commute, keeping the lights on, providing access to clean water or transforming skylines, our work helps people and communities thrive.Our clients trust us to bring together the best people, ideas, technical expertise and digital solutions to our work in transportation, buildings, water, the environment and new energy. We’re one global team – 50,000 strong – driven by a common purpose to deliver a better world. About Construction Management - AECOM TishmanSince 1898, AECOM Tishman has managed the construction of some of the world’s most iconic buildings. We employ a diversified preconstruction and construction management staff of structural, mechanical, electrical, and civil engineers; architects; technology specialists; scheduling and cost control personnel; and construction estimators and accountants. We provide expert consultation and guidance in all phases of a building project, from master-planning, preconstruction options evaluation and decision-making, to design review, estimating, and scheduling, through procurement, construction and occupancy. AECOM Tishman’s staff manages all consultants and contractors on a project, representing client interests throughout the project cycle. In total, AECOM Tishman has built more than 900 million square feet – including the tallest building in the Western Hemisphere, One World Trade Center in New York.Job DescriptionAECOM Tishman is seeking a graduated entry level Construction Project Engineer for our construction project in Boston, MA.  Enforces policies, procedures and related work rules as established by Field Management. Assists with compliance of safety program that creates a safe and health work environment through the job site and adheres to OSHA safety and record keeping requirements. Ensures safety standards and requirements are adhered to by crafts/trades, laborers and others when in the assigned operational area as well as ensure tools and equipment are in safe condition and operated safely.Prepares reports, as required, and keeps supervisors informed on progress of overall assigned activities.Under guidance of Superintendent or Project Manager, monitors work performance and of subcontractors to ensure project plans and schedules are followed. This includes, but is not limited to, reviewing construction methods, schedules, manning charts, material and equipment requirements, etc...Ensures compliance with all internal and external record keeping requirements, with particular emphasis on accurate, properly coded timecards and accurately codes, fully priced material delivery tickets.Uses current construction management system to perform record-keeping tasks including, composing daily diaries, maintaining project logs and retrieving RFIs, submittal logs and agreements.Provides assistance to assigned contractors in scheduling issues.Monitors the project pre-plan which includes a CPM schedule, work sequences, manpower utilization, material handling and storage requirements and equipment use.When requested, interfaces with client, architect and design professionals to ensure compliance to design intent and client satisfaction.Contribute to building good communications between field management, project management, estimating, procurement, suppliers, vendors, and specialty contractors to ensure construction complies with plans, specifications and company quality standards and that the project is completed on time and within budget.Responsible for continuously expanding and updating professional knowledge and honing training skills in order to enhance individual and team innovation and productivity.QualificationsMINIMUM REQUIREMENTS:BA/BS Engineering, Construction Management or relevant curriculum or demonstrated equivalency of experience and/or education. PREFERRED QUALIFICATIONS:Internship experience in construction of large scale projects from a large general constructor.    Experience working on a live construction site. Familiarity with construction documentation such as reports, safety recording keeping, quality control plans, etc.  Able to follow directions and interact with all levels of management on working construction project.Proficiency in Microsoft Office products.Experience engaging with multiple trades on a complex construction project.Additional InformationThis position does not include sponsorship for United States work authorization.This position does not include relocation benefits.With infrastructure investment accelerating worldwide, our services are in great demand, and there’s never been a better time to be at AECOM! Join us, and you’ll get all the benefits of being a part of a global, publicly traded firm – access to industry-leading technology and thinking and transformational work with big impact and work flexibility.AECOM provides a wide array of compensation and benefits programs to meet the diverse needs of our employees and their families. We also provide a robust global well-being program. We’re the world’s trusted global infrastructure firm, and we’re in this together – your growth and success are ours too.As an Equal Opportunity Employer, we believe in each person’s potential, and we’ll help you reach yours.Join us and let’s get started.

Part Time / Full Time
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Project Controls Analyst
AECOM
location-iconBoston MA

Job DescriptionCompany DescriptionAt AECOM, we’re delivering a better world. We believe infrastructure creates opportunity for everyone. Whether it’s improving your commute, keeping the lights on, providing access to clean water or transforming skylines, our work helps people and communities thrive. Our clients trust us to bring together the best people, ideas, technical expertise and digital solutions to our work in transportation, buildings, water, the environment and new energy. We’re one global team – 47,000 strong – driven by a common purpose to deliver a better world.About Construction Management - AECOM TishmanSince 1898, AECOM Tishman has managed the construction of some of the world’s most iconic buildings. We employ a diversified preconstruction and construction management staff of structural, mechanical, electrical, and civil engineers; architects; technology specialists; scheduling and cost control personnel; and construction estimators and accountants. We provide expert consultation and guidance in all phases of a building project, from master-planning, preconstruction options evaluation and decision-making, to design review, estimating, and scheduling, through procurement, construction and occupancy. AECOM Tishman’s staff manages all consultants and contractors on a project, representing client interests throughout the project cycle. In total, AECOM Tishman has built more than 900 million square feet – including the tallest building in the Western Hemisphere, One World Trade Center in New York.Job DescriptionAECOM Tishman is seeking an experienced Project Control Analyst for our iconic construction project in Boston, MAJob Description:Works with company financial systems and processes.Develops proficiency in the use of company cornerstone systems and provides cost data in formats necessary to control the project.Assists in analyzing and using financial data to identify key project issues.Able to use drawings and specifications in the establishment of project baseline dataDevelops knowledge of accounting principles.Assists in assembling data for trending and forecasting.Prepares analysis of progress trends and cost impact. May participate in reviewing and approving contractor invoices.Collects and analyzes data on manpower, labor hour, and labor cost requirements versus budget limitations.Collects and analyzes data for tracking actual cost to funding limitations.Assists in tracking purchase orders and subcontract commitments and expenditures.Supports the project reporting process as required.Participates in project cost review meetings.Gathers data for procedure development.QualificationsMinimum Requirements:BA/BS + 4 years of relevant project controls experience with a construction or A/E firm demonstrated equivalency of experience and/or education.Preferred:4 years of experience with project controls from a larger general contractor.Familiarity with construction documentation relevant to project controls.Able to follow directions and interact with all levels of management working on active construction projects.Proficiency with Microsoft Office (Word, Excel, Teams, Outlook).Proficiency with Procore.Additional InformationThis position does not include sponsorship for United States work authorization.This position does not include relocation benefits.All your information will be kept confidential according to EEO guidelines.With infrastructure investment accelerating worldwide, our services are in great demand, and there’s never been a better time to be at AECOM! Join us, and you’ll get all the benefits of being a part of a global, publicly traded firm – access to industry-leading technology and thinking and transformational work with big impact and work flexibility.AECOM provides a wide array of compensation and benefits programs to meet the diverse needs of our employees and their families. We also provide a robust global well-being program. We’re the world’s trusted global infrastructure firm, and we’re in this together – your growth and success are ours too.As an Equal Opportunity Employer, we believe in each person’s potential, and we’ll help you reach yours.Join us and let’s get started.

Part Time / Full Time
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Co-op, Chemical Biology & Proteomics
Biogen
location-iconCambridge MA

Job DescriptionCompany DescriptionAt Biogen, our mission is clear - we are pioneers in neuroscience. Biogen discovers, develops, and delivers worldwide innovative therapies for people living with serious neurological and neurodegenerative diseases. Together, our employees create, commercialize, and manufacture transformative therapies for our patient population.   We at Biogen are committed to building on our culture of inclusion and belonging that reflects the communities where we operate and the patients who we serve. We are focused on strengthening our foundation to advance our overall Diversity, Equity and Inclusion (DE&I) strategy and, most importantly, ensure all our employees feel included. As an intern or co-op at Biogen, you can expect to be placed on a real project, under the guidance of experience professionals and subject matter experts who are invested in your career and academic growth. We also ensure that you have plenty of opportunities to build your network, learn more about our organization through weekly lunch and learns led by leaders from across the company, and join us for several fun events. Job DescriptionThis application is for a 6-month student role from July - December 2023. Resume review begins in January 2023. The Chemical Biology and Proteomics (CBP) group works on a wide range of research projects that support the Biogen pipeline by designing and executing robust and reproducible bioanalytical assays. CBP capabilities include but are not limited to higher-resolution interrogation of novel biology and the molecular mechanism of action of molecules that help advance the best drug candidates into the clinic. Position Description Biogen is searching for a highly motivated and collaborative Summer Co-op to join the Chemical Biology and Proteomics (CBP) group within the Biotherapeutics and Medicinal Sciences department (BTMS). Our group develops and applies advanced proteomics methods in supporting therapeutics characterization (target engagement, lead compound selectivity and drug MOA, etc.), target biology and validation, and advancement of drug discovery tools. Technology development is an essential and fundamental component of the group function to support the Biogen portfolio. The Co-op will adapt their chemical biology and mass spectrometry techniques skills to answer biomedically focused research questions in cutting-edge laboratories for drug discovery.  A prospective candidate will perform the following tasks including but not limited to: Characterize and evaluate of chemical probes in biological systems for target identification, target engagement and selectivity profiling  Combine the application of chemical biology methods and proteomics techniques for cellular protein activity profiling and mechanism of action (MOA) study Proteomics sample preparation, proteomics data processing and bioinformatics analysis. Operation and instrumentation of modern LC-MS systems Work with mentoring scientists on method development and troubleshooting  Maintain good written records of laboratory procedures, attend group/team meetings and present at an internal session at the end of the program Engage and interact with scientists within and outside the team QualificationsGood communication and inter-personal skills Familiarity with basic chemical biology concepts and techniques, such as click-chemistry, activity-based protein profiling, photochemical crosslinking and chemoproteomics. Experience in the following skills: Basic laboratory techniques, including pipetting, protein quantification, cell lysis, click chemistry, gel electrophoresis, and Western blotting.  Mammalian cell/tissue culture expertise, including practical experience with transfection (stable/transient overexpression and knockdown by lentiviral transduction and plasmid transfection). Affinity enrichment or immunoprecipitation workflows from mammalian cell lysate. Familiarity or previous expertise with mass spectrometry, LC-MS/MS, and quantitative proteomics.  Perform data analysis and visualization using appropriate software Efficiently manage time to enable pursuit of multiple objectives in parallel To participate in the Biogen Co-op Program, students must meet the following eligibility criteria: Legal authorization to work in the U.S. At least 18 years of age prior to the scheduled start date Be currently enrolled in an accredited college or university Education Currently enrolled in a Master’s or Ph.D. program in chemical biology, chemistry, biochemistry, or a related discipline. Location Cambridge, MA Additional InformationAll your information will be kept confidential according to EEO guidelines.

Part Time / Full Time
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Project Manager - Federal Programs (Defense Facilities)
AECOM
location-iconBoston MA

Job DescriptionCompany DescriptionAt AECOM, we’re delivering a better world.We believe infrastructure creates opportunity for everyone. Whether it’s improving your commute, keeping the lights on, providing access to clean water or transforming skylines, our work helps people and communities thrive.Our clients trust us to bring together the best people, ideas, technical expertise and digital solutions to our work in transportation, buildings, water, the environment and new energy. We’re one global team – 47,000 strong – driven by a common purpose to deliver a better world.Here, you will have freedom to grow in a world of opportunity.We will give you the flexibility you need to do your best work with hybrid work options. Whether you’re working from an AECOM office, remote location or at a client site, you will be working in a dynamic environment where your integrity, entrepreneurial spirit and pioneering mindset are championed.You will help us foster a culture of equity, diversity and inclusion – a safe and respectful workplace, where we invite everyone to bring their whole selves to work using their unique talents, backgrounds and expertise to create transformational outcomes for our clients.We will encourage you to grow and develop your career with us through our technical and professional development programs and diverse career opportunities. We believe in leadership at all levels. No matter where you sit in the organization you can make a lasting impact on the projects you work on, the teams and committees you join and our business.We offer competitive pay and benefits, well-being programs to support you and your family, and the development resources you need to advance your career.When you join us, you will connect and collaborate with a global network of experts – planners, designers, engineers, scientists, consultants, program and construction managers – leading the change toward a more sustainable and equitable future. Join us and let’s get started. Job DescriptionAECOM has an excellent career opportunity for a creative, highly talented Project Manager for immediate employment in our Boston, MA location which serves as our home office to support national defense-related programs throughout the US and internationally. In this role the successful candidate will apply their experience towards supporting the US Army Corps of Engineers for Government Missile Defense Agency Programs and other high-profile clients. We help shape the world around us — from complex building designs such as radar and tactical support facilities, administrative, operation and maintenance facilities to large campus style projects.The candidate will manage project(s) with up to $15M contract value and $5M annual gross revenue. Manage and lead all technical, financial, and client satisfaction areas using consistent processes and tools. May include management of small to large teams across business lines, in remote locations and/or management of subcontractors.  The project manager will act as the primary point of contact with the client and with full responsibility for project delivery.About AECOMAt AECOM, we believe infrastructure creates opportunity for everyone. Whether it’s improving your commute, keeping the lights on, providing access to clean water or transforming skylines, our work helps people and communities thrive.We take on the most complex challenges and pioneer innovative, iconic solutions that push the limits of what’s possible – the world’s longest cable-stayed bridge, record-breaking sports events, the largest greenfield port development mega project, life-sustaining and disaster recovery programs, and the tallest tower in the Western Hemisphere.On projects spanning transportation, buildings, water, governments, energy and the environment, we deliver professional services throughout the project lifecycle.We are proud to be recognized for excellence:Fortune’s World’s Most Admired Companies – 2014-2020#1 in Transportation and General Building in Engineering-News Record's 2019 “Top 500 Design Firms” and #1 2019 “Top 200 Environmental Firms”VIQTORY 2020 Military Friendly® Gold Employer Perfect score on the Human Rights Campaign Foundation's Corporate Equality Index for 2017-2019The responsibilities of this position include, but are not limited to:Supporting the Program Manager in the development of proposals for new workSupporting Program Manager on financials on future growth opportunitiesManaging project(s) with up to $15M contract value and $5M annual gross revenue in support of U.S. Government Missile Defense Agency ProgramsPlanning, directing and supervising all operations included in medium to large-sized projects with moderate risk and technical complexityManaging and leading all technical, financial and client satisfaction areas using consistent processes and toolsMay include managing diverse teams across business lines, in remote locations and/or management of subcontractorsServe as primary point of contact with client with full responsibility for project delivery (quality, budget, and schedule)Travel required for durations typically up to one week to locations worldwide (e.g.,  Alaska, Greenland, Hawaii, Poland, Qatar, and Saudi Arabia)Participating in building and maintaining positive relationships with internal and JV partners as well as external client and stakeholder partnersQualificationsMinimum Requirements:Bachelor's degree in Engineering or ArchitectureProfessional Engineer (PE) license, Registered Architect (AIA) with NCARB Council CertificationSix (6) years of work experience in engineering or architecture with 3 years of relevant project management experienceMust be a highly motivated self-starter with solid writing and verbal communication skillsExperience in developing design reports, drawings, and specificationsProficient in MS Suite, SharePoint (or similar collaboration tools) and remote communications applications such as Teams, Zoom, etc.Experience in managing subcontractorsExperience in services during construction, including answering RFI’s and reviewing submittalsDue to the nature of this work, U.S. citizenship is requiredPreferred Qualifications:Ten (10) years of work experience in engineering or architecture with five (5) years of relevant project management experienceProfessional Engineer (PE) license, Registered Architect (AIA) with NCARB Council Certification (or ability to earn Certificate within one year)Experience managing projects for the US Army Corps of Engineers with knowledge of UFC Standards, ProjNet, and project controls (scheduling and cost/budget management)Security Clearance (or ability to obtain)Basic familiarity with AutoCAD, BIM, etc.Project Management Professional (PMP), or related qualificationAdditional InformationAll your information will be kept confidential according to EEO guidelines.Here, you will have freedom to grow in a world of opportunity.We will give you the flexibility you need to do your best work. Whether you’re working from an AECOM office, remote location or at a client site, you will be working in a dynamic environment where your integrity, entrepreneurial spirit and pioneering mindset are championed.With infrastructure investment accelerating worldwide, our services are in great demand, and there’s never been a better time to be at AECOM! Join us, and you’ll get all the benefits of being a part of a global, publicly traded firm – access to industry-leading technology and thinking and transformational work with big impact and work flexibility.We will encourage you to grow and develop your career with us through our technical and professional development programs and diverse career opportunities. We believe in leadership at all levels. No matter where you sit in the organization you can make a lasting impact on the projects you work on, the teams and committees you join and our business.AECOM provides a wide array of compensation and benefits programs to meet the diverse needs of our employees and their families. We also provide a robust global well-being program. We’re the world’s trusted global infrastructure firm, and we’re in this together – your growth and success are ours too.As an Equal Opportunity Employer, we believe in each person’s potential, and we’ll help you reach yours.Join us and let’s get started.

Part Time / Full Time
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Clinical Reimbursement Specialist
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Part Time / Full Time
location-iconWoburn MA
Job Description
Next Step Healthcare is seeking an experienced Clinical Reimbursement Specialist to support our MDS/MMQ teams in Massachusetts.

The Clinical Reimbursement Specialist provides extensive training, analysis, advice and consultation to the facilities and teams within his/her area of responsibility. Ensures compliance with federal and state regulations, as well as Company policy and procedures regarding state case mix/Medicare and Managed Care payment systems. Monitors, consults, and makes effective recommendations for changes and modifications to existing facility processes, systems, policies, and practices which will assure efficient, effective and compliant state Medicaid/Medicare/Managed Care payment performance.

Full-time; home office based position with 3-4 travel days per week covering North Boston, Central & Western MA.

Job Functions include but are not limited to:

Provides consultation, training and support concerning the Medicare, Managed Care and state case mix payment system for the assigned area.
Analyzes systems and processes to determine that federal and state regulations as well as company policies and procedures are followed. Promotes compliance by performing periodic audits of MDS assessments, supporting documentation, and other relevant data.
Recognizes, advises and promotes facility best practices and systems for dealing with state case mix/Medicare and Managed Care payment systems.
Studies, analyze and reports period over period information and systems in order to identify trends and deviations from results in Medicare, Managed Care and State Case Mix Index and takes appropriate actions.
Works in conjunction with teams to resolve issues effecting deviations from expected results. Recommends changes and performs follow-up to ensure that those recommendations are effectively implemented and monitored for appropriateness.
Regularly communicates to management outside the facility on recommendations made to facility management to ensure proper implementation and follow-up.
Serves as a liaison between state and organization related to the state case-mix process, including electronic submission and state MDS requirements related to state payment.
Assists in the recruitment/interview process for MDS and MMQ vacancies.

Qualifications:

Licensed as a Registered Nurse in the State of Massachusetts
Three to Five years of clinical experience in a long-term care setting, which includes supervisory, administrative or consultative capacities.
Current knowledge of computer technology and systems.
Ability to work independently with minimal supervision and guidance.
Extensive knowledge of MDS and back-up documentation required and extensive knowledge of state grouper and calculator field relative to MDS and state payment.
Extensive knowledge of Medicare reimbursement, RUG IV system, compliance and eligibility.
Must be willing and able to travel extensively and maintain a valid driver’s license.

We offer competitive compensation and benefit plans including:

Vacation, sick and holiday pay
Medical, Dental, Vision Insurance
ST/LT Disability Insurance
Tuition Reimbursement
Life Insurance
401K

At Next Step Healthcare, we know that working in the healthcare industry is more than just a job – it’s a way of life reserved for the most compassionate, caring, and hard-working individuals. Are you ready to take the next step in your career? Apply today.

Next Step Healthcare is an equal opportunity employer. We embrace diversity and are committed to fostering an inclusive workplace for all employees.

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Clinical Reimbursement Specialist
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Part Time / Full Time
location-iconWoburn MA
Job Description
Next Step Healthcare is seeking an experienced Clinical Reimbursement Specialist to support our MDS/MMQ teams in Massachusetts.

The Clinical Reimbursement Specialist provides extensive training, analysis, advice and consultation to the facilities and teams within his/her area of responsibility. Ensures compliance with federal and state regulations, as well as Company policy and procedures regarding state case mix/Medicare and Managed Care payment systems. Monitors, consults, and makes effective recommendations for changes and modifications to existing facility processes, systems, policies, and practices which will assure efficient, effective and compliant state Medicaid/Medicare/Managed Care payment performance.

Full-time; home office based position with 3-4 travel days per week covering North Boston, Central & Western MA.

Job Functions include but are not limited to:

Provides consultation, training and support concerning the Medicare, Managed Care and state case mix payment system for the assigned area.
Analyzes systems and processes to determine that federal and state regulations as well as company policies and procedures are followed. Promotes compliance by performing periodic audits of MDS assessments, supporting documentation, and other relevant data.
Recognizes, advises and promotes facility best practices and systems for dealing with state case mix/Medicare and Managed Care payment systems.
Studies, analyze and reports period over period information and systems in order to identify trends and deviations from results in Medicare, Managed Care and State Case Mix Index and takes appropriate actions.
Works in conjunction with teams to resolve issues effecting deviations from expected results. Recommends changes and performs follow-up to ensure that those recommendations are effectively implemented and monitored for appropriateness.
Regularly communicates to management outside the facility on recommendations made to facility management to ensure proper implementation and follow-up.
Serves as a liaison between state and organization related to the state case-mix process, including electronic submission and state MDS requirements related to state payment.
Assists in the recruitment/interview process for MDS and MMQ vacancies.

Qualifications:

Licensed as a Registered Nurse in the State of Massachusetts
Three to Five years of clinical experience in a long-term care setting, which includes supervisory, administrative or consultative capacities.
Current knowledge of computer technology and systems.
Ability to work independently with minimal supervision and guidance.
Extensive knowledge of MDS and back-up documentation required and extensive knowledge of state grouper and calculator field relative to MDS and state payment.
Extensive knowledge of Medicare reimbursement, RUG IV system, compliance and eligibility.
Must be willing and able to travel extensively and maintain a valid driver’s license.

We offer competitive compensation and benefit plans including:

Vacation, sick and holiday pay
Medical, Dental, Vision Insurance
ST/LT Disability Insurance
Tuition Reimbursement
Life Insurance
401K

At Next Step Healthcare, we know that working in the healthcare industry is more than just a job – it’s a way of life reserved for the most compassionate, caring, and hard-working individuals. Are you ready to take the next step in your career? Apply today.

Next Step Healthcare is an equal opportunity employer. We embrace diversity and are committed to fostering an inclusive workplace for all employees.

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