- Otsuka America Pharmaceutical Inc. (Sacramento, CA)
- …(T0 - T1) or early development (phase 1) assets either within Medical Affairs , Regulatory Affairs , or Clinical Development is preferred. + Minimum of 7+ ... disorders, we are seeking a skilled and experienced Medical Director of CNS Early Assets, Global Medical Affairs...evidence, US and global commercial teams, market access, and regulatory affairs , to ensure integrated global strategies… more
- Amneal Pharmaceuticals (Piscataway, NJ)
- …Global Regulatory Strategies: Formulate and lead global CMC and clinical regulatory strategies for Biologics, Biosimilars, and Small Molecules.Ensure ... Description: Regulatory expert in the area of Biosimilar/BLA submissions...of Biosimilar/BLA submissions including strategize, compile, review and manage/lead regulatory submissions. Subject matter expert in the area of… more
- CVS Health (Springfield, IL)
- …CVS Health, a Fortune 6 company, has an outstanding opportunity for a Medical Director (Medical Affairs ). This is a remote based, work from home opportunity. ... The Medical Affairs department provides clinical business support to...Enterprise Analytics, Compliance, Legal, Accreditation) and clients. The Medical Director (Medical Affairs ) will report into the… more
- Merck (Rahway, NJ)
- **Job Description** The Global Senior Director of Medical Affairs (GDMA) for Melanoma coordinates the development of the Global Scientific and Medical Affairs ... edge of therapeutic and patient care advances. The GDMA coordinates medical affairs activities to resolve regulatory , reputational, ethical, and other asset… more
- Lilly (Indianapolis, IN)
- …"patient journey" and the strategic plan for the compound), medical support for regulatory affairs and interactions with government agencies (medical support for ... relevant clinical experience, the Cardiometabolic Health Business Unit - Global Medical Affairs Sr. Director is an integral member of the medical affairs… more
- Veterans Affairs, Veterans Health Administration (Hines, IL)
- Summary The Clinical Laboratory Scientist (CLS) supervises at least one staff member at the GS-14 grade level. The CLS exercises a full range of supervisory ... and assessing work of subordinate staff. The CLS serves as a VISN-level director for PLM, provides overall technical and administrative direction to the Clinical… more
- AbbVie (North Chicago, IL)
- …interpretation, and reporting of scientific content of protocols, Investigator Brochures, Clinical Study Reports and regulatory submissions and responses. + ... Has overall responsibility for oversight of the Medical Affairs -led clinical studies, monitoring overall study integrity and review, interpretation and… more
- Regeneron Pharmaceuticals (Sleepy Hollow, NY)
- …a typical day might include:** The Manager position within the Regulatory Affairs department requires the ability to apply clinical development knowledge in ... relevant stakeholders, typically carrying out the responsibilities with guidance from the Regulatory Affairs , Advertising and Promotion Director . The Manager… more
- Merck (Hartford, CT)
- **Job Description** The Executive Director (ED) for US Medical Affairs (USMA) understands Our Company's enterprise level strategies and leads cross-functionally ... with the Global Medical and Scientific Affairs Therapeutic Area (GMSA TA) teams to translate Global...including tactical execution by the field Regional Medical Scientific Director (RMSD) teams and is accountable for ensuring field… more
- Sumitomo Pharma (Cheyenne, WY)
- …Director , Medical Strategy (Prostate Cancer) will be a key member of the Medical Affairs team reporting to the Senior Director , Medical Affairs Strategy. ... initiatives and advance patient advocacy efforts to ensure that Medical Affairs activities align with patient focused programs. **Job Duties and Responsibilities**… more