The Postdoctoral Fellow will be responsible for coordinating clinical trials and studies, ensuring that all research activities comply with regulatory standards, protocols, and guidelines. Collaborate closely with clinical sites in multicenter studies, other principal investigators, and research team members to uphold the integrity and quality of clinical data. The Postdoctoral Researcher will gain knowledge of clinical research methodologies, including study design, data collection, and analysis. Additionally, develop an understanding of the ethical principles and guidelines governing clinical research, such as informed consent, patient confidentiality, and the procedures for obtaining institutional review board (IRB) approval. Also, participate in the development and refinement of research protocols to ensure alignment with scientific standards and regulatory requirements. *LEARNING OBJECTIVES* The objectives include acquiring knowledge about clinical research methodologies, encompassing hypothesis generation, study design, data collection, and analysis. It also involves understanding the ethical principles and guidelines that govern clinical research, such as informed consent, patient confidentiality, and the processes for obtaining Institutional Review Board (IRB) approval. Participation in the development and refinement of research protocols is expected, ensuring they comply with scientific standards and regulatory requirements. Furthermore, engagement in manuscript preparation and scientific writing shall be actively pursued. *ELIGIBILITY REQUIREMENTS* US or Foreign Medical graduate who has completed Step 1 and 2 of the USMLE boards at the time of application. *POSITION INFORMATION* MD Anderson offers full-time postdoc positions with a https://www.utsystem.edu/offices/employee-benefits/ut-retirement-program/voluntary-retirement-programs, tuition benefits, educational opportunities, and individual and team recognition08/31/2025