- Veterans Affairs, Veterans Health Administration (San Antonio, TX)
- …their team. Responsibilities Duties may include but are not limited to: Global : a. The incumbent must possess necessary interpersonal skills to function effectively ... maintains ASHP accreditation for the program when serving as a Residency Program Director . Performs other duties as required. Work Schedule: Monday - Friday, 8:00am… more
- Abbott (Pleasanton, CA)
- …Heart Failure. We have an exciting opportunity for a seasoned leader to join our Global Clinical and Regulatory Affairs team within the Heart Failure ... Division (HFD) as the Global Director of Clinical Insights Development. This...by working closely with internal stakeholders (R&D, Marketing, Clinical Affairs , Regulatory Affairs , Medical … more
- Otsuka America Pharmaceutical Inc. (Santa Fe, NM)
- …documents, including INDs, IBs, clinical study reports, and NDAs/BLAs. + Collaborate with regulatory affairs on interactions with global health authorities. ... on the large global clinical trials and regulatory filing activities. The Senior Director , GCD...trial implementation and management. + Complete understanding of the global regulatory requirements. + Working knowledge of… more
- Bristol Myers Squibb (Princeton, NJ)
- …and in their personal lives. Read more: careers.bms.com/working-with-us . The Senior Director for Milvexian Global Medical Strategy will provide deep disease ... planning, development, and implementation of the medical plan. The Director will report to the Executive Director ,...in Phase IIIb/IV trials and real-world evidence programs across Global Medical Affairs + Review and develop… more
- Otsuka America Pharmaceutical Inc. (Little Rock, AR)
- …Actions (CAPA), Deviations, and Change Control** , ensuring compliance with global regulatory requirements and internal standards. The successful candidate ... **Job Summary** The Associate Director , Global Product Quality - GMP...alignment with corporate quality objectives + Cross-functional Leadership:Collaborate with Regulatory Affairs , Technical Operations, Manufacturing, and Supply… more
- Takeda Pharmaceuticals (Boston, MA)
- …Payer Marketing and Market Access, Global Evidence and Outcomes, Medica Affairs , Clinical Development, Regulatory Affairs , Biostatistics, Global ... Market Access, Pricing, Advocacy, Biostatistics, Global Evidence and Outcomes, Medical Affairs , Clinical Science, Legal, Regulatory + OBU 10, EUCAN, GEM… more
- Takeda Pharmaceuticals (Boston, MA)
- …with key functions across Takeda Oncology including Translational Medicine, Clinical Sciences, Global Regulatory Affairs , the Oncology Business Unit ... and empower you to shine? Join us as a Director , Global Program Management in our Cambridge...data integration. + Understanding of key considerations relevant to global regulatory requirements + Experience developing team… more
- Takeda Pharmaceuticals (Boston, MA)
- …to the best of my knowledge. **Job Description** **About the role:** The Director , Global Medical Communications, Immunology, is a dynamic, strategic role within ... Global Medical Affairs responsible for driving the...review process for medical materials; Work with Legal and Regulatory colleagues to resolve questions and provide leadership in… more
- ThermoFisher Scientific (Wilmington, NC)
- …and benefit-risk management strategies + Closely collaborate with stakeholders internally (eg Regulatory Affairs , clinical development, medical affairs ) and ... meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission...safety contributions for the preparation of relevant sections of regulatory submission documents globally (eg ISS, SCS, narratives) for… more
- Novo Nordisk (Plainsboro, NJ)
- …Team, at the discretion of the Executive Director + Represent NNI Medical Affairs on Global Core Medical Team (CMT) + Collaborate with HEOR to provide ... Area in certain instances, at the discretion of Executive Director of Medical Affairs . Assists the Senior...Local Labeling Committee (LLC) and provide medical input to Regulatory Affairs Physical Requirements 20-30% overnight travel… more