Featured Job
-
Job Removed or Not Found
Related Jobs
- Eisai, Inc (Nutley, NJ)
- …Develop medical strategy for major products and/or indications and provide critical medical input into the lifecycle management strategies in responsible therapeutic
- Genmab (NJ)
- …Identify key thought leaders and establish, foster, cultivate, and maintain relationships with healthcare providers (HCPs) in academic and community centers within
- Eisai, Inc (Nutley, NJ)
- …without regard to race, color, religion, gender, age, national origin, citizenship status, marital status, sexual orientation, gender identity, disability or veteran
- Merck & Co. (North Wales, PA)
- …also include development of American Managed Care Pharmacy (AMCP) dossiers for US payers and Global Value Dossiers for use by local subsidiaries in their HTA
- Legend Biotech USA, Inc. (Baton Rouge, LA)
- …Headquartered in Somerset, New Jersey, we are developing advanced cell therapies across a diverse array of technology platforms, including autologous and allogenic
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …Leads the development of the US Medical Affairs strategy and execution of the US Medical Affairs plan for select indications/projects related to evidence generation,
- Merck & Co. (Rahway, NJ)
- …Vice President, Regulatory Affairs, General Medicine, will contribute to the mission and vision of the Global Regulatory Affairs and Clinical Safety (GRACS) function of
- Eisai, Inc (Nutley, NJ)
- …The Executive Director, Regulatory Affairs will provide leadership and direction for the global regulatory aspects of Eisai's products under development and post approval
- Merck & Co. (Upper Gwynedd, PA)
- …include, but are not limited to:Regulatory Responsibilities: Serve as a CMC Product Lead for assigned products and be accountable for the delivery of all regulatory
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …for Development : Manages multiple CMC development projects. Leads submission teams with supervision. Acts as point of contact to cross-functional teams on US/EU RA CMC