- Sanofi (Morristown, NJ)
- Job Title: Associate Director - Principal Medical Writer Location: USA, Remote. Proximity to Cambridge/Boston, MA or Morristown, NJ is highly desirable for ... be critical in helping our teams accelerate progress. The Principal Medical Writer is a key member...the clinical opinion, as defined by the Clinical Study Director and the Therapeutic Department Head, is presented accurately… more
- Sanofi (Morristown, NJ)
- Job Title: Principal Medical Writer Associate Director Location : USA, Remote. Proximity to Cambridge/Boston, MA or Morristown, NJ is highly desirable ... be critical in helping our teams accelerate progress. Global Medical writing and Document management serves to generate timely,...partners About You Core Experience : Six+ years as medical writer or equivalent specialist role Proven track record… more
- Merck & Co. (Rahway, NJ)
- …areas and routes of administration, including inhalation, implantation, and injection.The Associate Principal Scientist will lead the definition and execution ... the clinical instruction(s) and commercial market approval(s) of combination products. Principal ResponsibilitiesLead, set direction, align with key stakeholders, and… more
- Merck & Co. (Rahway, NJ)
- …BARDS Real-World Evidence (RWE) Capabilities & Analytics team is looking for an Associate Director , Data Strategy & Partnerships with expertise in data strategy, ... to enable the discovery, development, regulatory approval, manufacturing, and marketing of medical drugs and vaccines for the benefit of patients and global human… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Senior Director (Sr. Principal Scientist) has primary responsibility for the planning and directing clinical research activities involving new ... and manufacturing to manage clinical development projects; and assist the Executive Director and/or Associate Vice President in ensuring that appropriate… more
- Organon & Co. (Jersey City, NJ)
- …Director in Organon Regulatory Chemistry, Manufacturing and Controls (CMC), the Associate Principal Scientist is responsible for developing and implementing ... in accordance with global regulations and guidances, and Organon procedures. The Associate Principal Scientist will lead the preparation and submission of… more
- Organon & Co. (Jersey City, NJ)
- …Reporting to the Director in Organon Regulatory CMC,?the Associate Principal Scientist is responsible for?developing and?implementing Regulatory Chemistry, ... products in accordance with global regulations and?guidance, and?Organon procedures.? The Associate Principal Scientist will lead the?preparation and submission… more
- Sanofi Group (Morristown, NJ)
- **Job Title:** Associate Director - Principal Medical Writer **Location:** USA, Remote. Proximity to Cambridge/Boston, MA or Morristown, NJ is highly ... be critical in helping our teams accelerate progress. The Principal Medical Writer is a key member...the clinical opinion, as defined by the Clinical Study Director and the Therapeutic Department Head, is presented accurately… more
- Sanofi Group (Morristown, NJ)
- **Job Title:** Principal Medical Writer Associate Director **Location** : USA, Remote. Proximity to Cambridge/Boston, MA or Morristown, NJ is highly ... be critical in helping our teams accelerate progress. Global Medical writing and Document management serves to generate timely,...**About You** **Core Experience** : + Six+ years as medical writer or equivalent specialist role + Proven track… more
- Merck (Rahway, NJ)
- …areas and routes of administration, including inhalation, implantation, and injection. The Associate Principal Scientist will lead the definition and execution ... clinical instruction(s) and commercial market approval(s) of combination products. ** Principal Responsibilities** + Lead, set direction, align with key...CFR 820 + 21 CFR 210/ 211 + EU Medical Device Regulation + USP <1> + USP <697>… more
