- Merck (Rahway, NJ)
- …Director , Combination Product Regulatory CMC - (R5)** This Principal Scientist position is equivalent to a Director position. Under direction from the ... Combination Product Regulatory CMC Team Leader, the Principal Scientist is responsible for executing in the Regulatory CMC space. Leveraging demonstrated… more
- Merck (Rahway, NJ)
- …Description** **Role Summary** + Under the guidance of a senior leader, a Principal Scientist / Director , has primary responsibility for developing value ... to reimbursement and market access, and provides input into clinical, regulatory , payer/access, marketing and evidence generation strategies and programs + In… more
- Merck (Rahway, NJ)
- …to reimbursement and market access, and provide input into clinical, regulatory , payer/access, marketing and evidence generation strategies and programs. + In ... collaboration with internal teams and external partners, design studies, author study protocols, develop measurement questionnaires, case report forms, data analysis plans, final study reports, scientific presentations, and publications. + Responsible for… more
- Merck (Rahway, NJ)
- **Job Description** The Director ( Principal Scientist ) has primary responsibility for the planning and directing of clinical research activities involving ... cycle of clinical development, including study design, placement, monitoring, analysis, regulatory reporting, and publication. Specifically, the Director may be… more
- Merck (Rahway, NJ)
- **Job Description** The Director ( Principal Scientist ) has primary responsibility for the planning and directing clinical research activities involving new ... cycle of clinical development, including study design, placement, monitoring, analysis, regulatory reporting, and publication. **Specifically, The Director May… more
- Merck (Rahway, NJ)
- …and pipeline products to produce safe, effective, innovative medicine. The Senior Principal Scientist /Senior Director is responsible for protocol development ... of manuscripts for publication in peer-reviewed journals. The Senior Director will also contribute to establishing Vaccine Clinical Development Strategies… more
- Merck (Rahway, NJ)
- …teams manage studies to provide the safety and efficacy data required for regulatory approval of potential new drugs, vaccines and new indications for existing ... technology and applying rigorous scientific and ethical standards. The Senior Director has primary responsibility for the planning and directing clinical research… 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… more
- City of New York (New York, NY)
- …compliance, and capital projects engineering and construction review and approval. Provide principal regulatory oversight and sanitary survey for the NYC ... including program management, resource allocation. Key program activities include regulatory inspections, issuance of commissioner's orders, bathing establishments engineering… more
- Bristol Myers Squibb (Madison, NJ)
- …acting on Clinical Trial data to support development, and + Serving as principal functional author for Regulatory submission, study reports, and publications + ... at work and in their personal lives. Read more: careers.bms.com/working-with-us . ** Director , Early Clinical Development (MD) - Hematology & Cell Therapy with Focus… more