- Organon & Co. (Jersey City, NJ)
- …**The Position ** Reporting to the Director in Organon Regulatory CMC, the Associate Principal Scientist is responsible for developing and implementing ... with global regulations and guidance, and Organon procedures. The Associate Principal Scientist will lead...products and be accountable for the delivery of all regulatory milestones for assigned products through the product lifecycle.… more
- Merck (Rahway, NJ)
- … documentation. Under the guidance of dCMC Regulatory Authoring Leadership, the Associate Principal Scientist , Regulatory Authoring Business Owner, ... and supply. A key workstream within this initiative is the auto-generation of regulatory filing sections, enabled by a dedicated application designed to create a… more
- Merck (Rahway, NJ)
- **Job Description** ** Associate Principal Scientist - Device Technical and Engineering Lead ( Associate Director Equivalent)** _Our company's Device ... ensure products and processes are developed in accordance with applicable regulatory , quality, company, and customer requirements. This position will lead… more
- Merck (Rahway, NJ)
- …art scientific methodologies and tools to enable the discovery, development, regulatory approval, manufacturing, and marketing of medical drugs and vaccines for ... Real-World Evidence (RWE) Capabilities & Analytics team is looking for an Associate Director, Data Strategy & Partnerships with expertise in data strategy, advanced… more
- Merck (Rahway, NJ)
- **Job Description** The **Clinical Director ( Principal Scientist )** has primary responsibility for the strategic planning and directing clinical research ... to pursue and subsequent study design, initiation, execution, monitoring, analysis, regulatory filing, and publication. **Specifically, The Clinical Director May Be… more
- Merck (Rahway, NJ)
- **Job Description** The Senior Director (Sr. Principal Scientist ) has primary responsibility for the planning and directing clinical research activities ... including development strategy, study design, initiation, execution, monitoring, analysis, regulatory reporting, and publication. **Specifically, the Senior Director May… more