Our postdoctoral training program is meticulously designed to equip future pharmacometricians and clinical pharmacologists with the expertise needed for thriving careers in industry, regulatory, or academia.
Through hands-on experience and mentorship from leading experts, trainees develop advanced skills in quantitative analysis, drug development, and regulatory science. Our comprehensive curriculum ensures that graduates are not only proficient in the latest methodologies but also adept at navigating the complex landscapes of pharmaceutical research and regulatory affairs, making them highly sought-after professionals in their respective fields.
About the Program
Throughout their time at the Center for Translational Medicine, postdoctoral fellows benefit from four primary functional areas:
Advanced Quantitative and Analytical Skills
- Training in State-of-the-Art Techniques: Master the latest pharmacometric methods, including population modeling, dose-response analysis, simulation techniques, and even new machine learning methodologies
- Data Analysis Proficiency: Develop expertise in analyzing complex datasets using advanced tools and software
- Application to Real-World Problems: Learn to apply quantitative analyses to solve critical issues in drug development, optimizing therapeutic strategies, and improving patient outcomes
Leaders in Pharmacometrics (LEAP) Program
The Leaders in Pharmacometrics (LEAP) program provides a comprehensive and dynamic approach to training in pharmacometrics and clinical pharmacology. This innovative program offers company-sponsored fellowships where fellows divide their time between the CTM and the sponsoring company. Through LEAP, CTM also collaborates with various organizations, including pharmaceutical companies, the US FDA, and the NIH, to present career opportunities to our network of over 200 graduates. If your organization is interested meeting our captive students, please reach out to Dr. Allison Dunn.
In-depth Regulatory Knowledge
- Understanding Regulatory Frameworks: Gain comprehensive knowledge of regulatory guidelines and requirements from agencies like the FDA, EMA, and other global regulatory bodies.
- Regulatory Submissions: Acquire hands-on experience preparing and reviewing documents for regulatory submissions, ensuring compliance and supporting successful drug approvals.
- Policy and Ethics: Learn the ethical considerations and policy implications of clinical pharmacology research, ensuring responsible and compliant scientific practice.
Professional Development and Networking
- Mentorship from Experts: Receive personalized guidance and career mentorship from leading professionals in pharmacometrics and clinical pharmacology.
- Networking Opportunities: Build a robust professional network through interactions with industry leaders, academic researchers, and regulatory officials.
- Career Transition Support: Benefit from tailored career development resources, including workshops, seminars, and one-on-one coaching to facilitate a smooth transition into industry, regulatory, or academic roles.
Through the Gilead-UMB Fellowship program, I’m gaining hands-on experience to advance my skillset in PKPD modelling in a supportive, motivating and enriching academic environment.
Dr. Shams Ismaeil, current CTM-Gilead Fellow (2022-2024)