- Insmed Incorporated (San Diego, CA)
- …risk communication for assigned gene therapy development products as well as medical assessment of individual adverse event reports, generation, and review of ... more
- Merck & Co. (North Wales, PA)
- …Company to solicit and include the voices of patients in research, medical affairs, commercial, public policy, and manufacturing plans.The Patient Insights Lead will ... more
- Merck & Co. (Rahway, NJ)
- …providing strategic oversight, leadership for the technical transfer portfolio for medical devices and combination products, as well as combination product ... more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and ... more
- Merck & Co. (Rahway, NJ)
- …their knowledge of product and process development in the (bio)pharmaceutical and/or medical device industries to set tactical and strategic direction on programs ... more
- Novo Nordisk Inc. (Plainsboro, NJ)
- About the Department The Clinical, Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the ... more
- Novo Nordisk Inc. (Chicago, IL)
- About the Department The Clinical, Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the ... more
- Novo Nordisk Inc. (Plainsboro, NJ)
- About the Department The Clinical, Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the ... more
- Aequor (Atlanta, GA)
- …for managing regulatory documentation related to clinical evaluations, particularly for Medical Device Regulation (MDR) remediation and Post Production Risk Reviews ... more
- Genmab (NJ)
- …competitive trends that could impact profitable accessAnalyze formulary coverage, medical policies, utilization controls, formulary review practices, pathways, and ... more
- Aequor (West Greenwich, RI)
- …Job duties, under general direction: Perform LVN or RN level assessment and medical management of work related injury/illness Facilitate return to work and workers' ... more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and ... more
- Beckman Coulter Diagnostics (Miami, FL)
- …and standards including compliance with Food & Drug Administration (FDA), Medical Device Single Audit Program (MDSAP), ISO13485, European Union Medical ... more
- Novo Nordisk Inc. (Plainsboro, NJ)
- About the Department The Clinical, Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the ... more
- Taiho Oncology (Los Angeles, CA)
- …classes and product certifications. Attends and or displays, at all relevant medical congresses and meetings as needed. Can develop and execute strategies to ... more
- Lundbeck (Houston, TX)
- …in a distinct geographical region. The product portfolio currently includes both medical benefit and specialty distribution for infusion therapy. The RBD will ... more
- Lundbeck (Chicago, IL)
- …and procedures and FDA regulations regarding the promotion of pharmaceutical and medical products. Ability to apply knowledge of overall healthcare economy and ... more
- Aequor (Irvine, CA)
- …and control of manufacturing processes and post-market performance of medical devices. Responsibilities include collaborating with internal and external stakeholders ... more
- Novo Nordisk Inc. (Torrance, CA)
- …DCS maintains relationships with physicians, physician assistants, nurse practitioners, medical assistants, pharmacists, nurses and other paramedical customers and ... more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and ... more
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