- Bristol Myers Squibb (Princeton, NJ)
- …(Masters, PhD, PharmD, BSN, etc.) with at least 3+ years of Regulatory Affairs experience in the pharmaceutical industry. **Key Competency Requirements** ... in their personal lives. Read more: careers.bms.com/working-with-us . **Associate Director , Global Regulatory Strategy, Neuroscience** **Position Summary:** The… more
- Bayer (Cambridge, MA)
- …specialists, Translational Sciences, Pharmacometrics, Research, Clinical Development, Regulatory , Medical Affairs and Commercial/Marketing functions. ... **Senior Director Clinical Pharmacology Lead** The Clinical Pharmacology Lead...Pharmacokinetic/Pharmacodynamic including model-based drug development as evidenced by major Regulatory submission experience (eg NDAs, CTDs, INDs), scientific… more
- Abbott (Pleasanton, CA)
- …have an exciting opportunity for the right candidate to join our Global Clinical and Regulatory Affairs team within the Heart Failure Division (HFD) as the ** ... Our 114,000 colleagues serve people in more than 160 countries. **Job Title** ** Director , Clinical Insights Development** **Working at Abbott** At Abbott, you can do… more
- OPEN Health (New York, NY)
- Director , HEOR, MEDICAL COMMUNICATIONS Reports to Executive Director , Value Communications Job Summary OPEN Health brings together deep scientific knowledge, ... PharmD degrees - work strategically alongside our client partners in Medical Affairs , Health Economics and Outcomes Research (HEOR), Market Access, and Commercial… more
- Regeneron Pharmaceuticals (Tarrytown, NY)
- The Executive Medical Director , Hematology, will provide overall clinical scientific leadership for a classical hematology program and have responsibility for ... a clinical role model for the team and demonstrates outstanding clinical scientific knowledge applicable to hematology clinical research. The Executive Medical … more
- J&J Family of Companies (Malvern, PA)
- …in their roles. + Collaborate cross-functionally with R&D, quality assurance, regulatory affairs , and manufacturing teams to integrate analytical strategies ... design of experiments and analytical characterization plans, ensuring compliance with regulatory requirements and leveraging deep scientific expertise in cell… more
- Sanofi Group (Cambridge, MA)
- **Job Title:** Director of Patient Marketing, Hemophilia A, US Rare Blood Disorders **Location:** Cambridge, MA **About the Job** Sanofi's Rare Blood Disorders ... diseases as well as several promising compounds in the pipeline. The Director , ALTUVIIIO Patient Marketing will be responsible for setting the strategic vision,… more
- Takeda Pharmaceuticals (Boston, MA)
- … regulatory requirements and guidelines. + Knowledge of other relevant regional regulatory nuances and requirements. + Knowledge of scientific principles and ... to bring life-changing therapies to patients worldwide. Join Takeda as Associate Director , Global Labeling Lead where you will be responsible for the development… more
- ICON Clinical Research (Raleigh, NC)
- Medical Director (Neurology)- Raleigh, NC- Remote ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an ... mission to shape the future of clinical development. We are currently seeking a Medical Director to join our diverse and dynamic team. As a Medical Director at… more
- Merck (North Wales, PA)
- …the guidance of a senior leader, an Associate Principal Scientist/Associate Director , has primary responsibility for planning/managing real world and economic ... is expected to work cross-functionally with clinical development, medical affairs , biostatistics, market access, commercial and country affiliates. The incumbent… more