- Novo Nordisk Inc. (Plainsboro, NJ)
- …learn quickly and leverage foundational competencies when entering new areas for advisory Applies best practice compliance processes, methods and tools ... the Department At Novo Nordisk, we're committed to building the best Ethics, Compliance & Privacy (ECP) team in the pharmaceutical industry. Operating at the highest… more
- Merck & Co. (North Wales, PA)
- Job DescriptionReports to the Director /Senior Director in the Office of Promotion and Advertising Review (OPAR)The Associate Director is responsible for the ... branch (APLB), including complex regulatory questions and submissions for advisory comment-Propose creative, effective, and compliant regulatory strategies and… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionTitle: Associate Principal Scientist/Associate Director , Outcomes ResearchRole SummaryUnder the guidance of a senior leader, an Associate Principal ... Scientist/Associate Director , has primary responsibility for planning/managing real world and economic evidence activities for in-line and pipeline products to meet… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …Oversees preparation and submission of draft introductory materials to OPDP for advisory comment Ensure company compliance with FDA requirements, including ... Are you ready to make a difference? The Position The Associate Director , Regulatory Affairs - Advertising & Promotion will provide strategic regulatory advice… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Executive Director , Value & Implementation (V&I), Global Medical and Scientific Affairs (GMSA) is accountable for the development and execution of ... TA dedicated global and regional directors and associate directors. The Executive Director , Value & Implementation (referred to as EDMA) engages with global… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionRole Summary: The Global Senior Director Medical Affairs (Sr GDMA), Hematology is responsible for driving the development and execution of the ... societies) about Our Company's emerging scienceOrganizes global expert input events ( advisory boards and group input meetings) to answer Our Company's questions… more
- Merck & Co. (North Wales, PA)
- Job DescriptionRole Summary: The US Regional Director Medical Affairs (RDMA), Prostate Cancer is responsible for driving the planning and execution of scientific & ... engagement with their national scientific leadersOrganizes regional expert input events ( advisory boards and group input meetings) to answer Our Company's questions… more
- Merck & Co. (Rahway, NJ)
- …role ensures the operational stability, maintenance, user configuration changes, performance, and compliance of an application or product in production.- As a member ... the product as well as work closely with CoP, Advisory , Delivery teams to define, document product information and...applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance Los… more
- Genmab (Plainsboro, NJ)
- …best, and authentic is essential to fulfilling our purpose.The RoleThe Associate Director , Key Accounts will shape, implement, and execute Key Account brand ... Genmab's first asset in hematology, EPKINLY. This critical role will report to the Director of Key Customer Strategy and be expected to work closely within the US… more
- Merck & Co. (Rahway, NJ)
- Job Description Role Summary: JOB DESCRIPTION: The Regional Director Medical Affairs (RDMA) is responsible for driving execution of scientific & medical affairs ... Our Company's questions regarding how to implement new indications: advisory boards and expert input forumsOrganizes regional symposia and...with the V&I Global H&N strategy As a regional director in oncology will also be responsible for the… more
