- Organon & Co. (Jersey City, NJ)
- **Job Description** **The Position** The Associate Principal Scientist ( Associate Director) is responsible for developing and implementing Regulatory ... with global regulations and guidances, and Organon procedures. The Associate Principal Scientist will lead...projects and be accountable for the delivery of all regulatory milestones for assigned products through the product lifecycle.… more
- Merck (Rahway, NJ)
- **Job Description** GRACS CMC - Associate Principal Scientist , CMC, R4 - Pharm Pre-approval Reporting to the Sr Director/Director/ Principal Scientist ... Pharmaceutical CMC is responsible for developing and implementing CMC regulatory strategies for our company's pharmaceutical pipeline products in accordance… more
- Bristol Myers Squibb (Princeton, NJ)
- …track record of high-quality scientific publications in relevant fields For the Sr. Principal Scientist position, the starting compensation for this job is a ... oncology. + Manage relationships with key internal stakeholders including regulatory , clinical and commercial and scientific communications and external… more
- Merck (Rahway, NJ)
- …Description** **Role Summary** + Under the guidance of a senior leader, an Associate Principal Scientist / Associate Director, has primary responsibility ... barriers to reimbursement and market access, and provide input into clinical, regulatory , payer/access, marketing and evidence generation strategy and programs + In… more
- Merck (Rahway, NJ)
- …process validation, second generation process development and authoring of regulatory submissions. Under the general scientific and administrative direction of ... next generation process development and characterization, process validation, and regulatory submission authoring **In this role, the successful candidate will… 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 ... the span of which range from individual clinical trials to world-wide regulatory application submissions and post marketing support. The incumbent is responsible for… 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