- Merck (Richmond, VA)
- **Job Description** **Global Senior Director of Medical Affairs for Thoracic Malignancies** + The Global Senior Director of Medical Affairs (GDMA) for ... edge of therapeutic and patient care advances. + The GDMA coordinates medical affairs activities to resolve regulatory , reputational, ethical, and other asset… more
- Merck (Richmond, VA)
- …_MUST_ reside in the territory. **Role Summary** + The Health Systems Oncology Medical Affairs Director (HSO MAD) is a therapeutic and disease expert who ... in a balanced and credible manner consistent with the regulatory environment and company's ethical standards. This role also...resource for the HSO MAD Team Lead, HSO Executive Director Medical Affairs , and other members of… more
- PLUS Communications (Arlington, VA)
- …nothing falls through the cracks. + Have experience synthesizing complex policy issues and/or regulatory affairs at the federal or state level. + Have a ... means more! PLUS Communications is looking for a Public Affairs (Healthcare), Senior Director to provide project...in this position includes: + Serving as a key advisor to the client - providing counsel on day-to-day… more
- PLUS Communications (Arlington, VA)
- …and media buying. PLUS means more! PLUS Communications is looking for a Director to provide public affairs and policy expertise, communications strategy and ... in this position includes: + Serving as a key advisor to the client - providing counsel on day-to-day...+ Crafting narratives by distilling complex energy policy and regulatory information into tangible messaging for a variety of… more
- Merck (Richmond, VA)
- …colleagues, GCTO Country Operations, other GCTO functional areas, Pharmacovigilance (PV), Global Regulatory Affairs and Clinical Safety (GRACS), IT, etc.) is ... teams manage studies to provide the safety and efficacy data required for regulatory approval of potential new drugs, vaccines and new indications for existing… more
- Merck (Richmond, VA)
- …partnership with GCTO (Global Clinical Trial Operations) country operations, finance, regulatory affairs , pharmacovigilance, legal and regional operations, HQ ... appropriately in a timely manner. + Collects, reviews, and monitors required regulatory documentation for study start-up, study maintenance and study close-out. +… more