- Merck & Co. (Rahway, NJ)
- … Principal Scientist , CMC, R4 - Pharm Pre-approval Reporting to the Sr Director / Director / Principal Scientist /Sr Principal Scientist in ... Pharmaceutical CMC is responsible for developing and implementing CMC regulatory strategies for our company's pharmaceutical pipeline products in accordance… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionRole SummaryUnder the guidance of a senior leader, an Associate Principal Scientist /Associate Director , has primary responsibility for ... reimbursement and market access, and provide input into clinical, regulatory , payer/access, marketing and evidence generation strategy and programsIn collaboration… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionRole Summary Under the guidance of an Executive Director , has primary responsibility for developing value evidence strategies, and planning/managing ... reimbursement and market access, and provides input into clinical, regulatory , payer/access, marketing and evidence generation strategies and programsIn… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionRole SummaryThe Principal Scientist / Director , Value & Implementation (V&I) Outcomes Research, position resides in the V&I organization, which ... reimbursement and market access, and provides input into clinical, regulatory , payer/access, marketing and evidence generation strategies and programs.In… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Director ( Principal Scientist ) has primary responsibility for the planning and directing of clinical research activities involving new or ... cycle of clinical development, including study design, placement, monitoring, analysis, regulatory reporting, and publication.Specifically, the Director may be… more
- Merck & Co. (Rahway, NJ)
- …process validation, second generation process development and authoring of regulatory submissions.-Under the general scientific and administrative direction of the ... Director in Biologics Cell Culture Sciences group and working...next generation process development and characterization, process validation, and regulatory submission authoringIn this role, the successful candidate will… more
- Merck & Co. (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… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Senior Director (Sr. Principal Scientist ) has primary responsibility for the planning and directing clinical research activities involving ... including development strategy, study design, initiation, execution, monitoring, analysis, regulatory reporting, and publication.Specifically, the Senior Director … more
- BioSpace (New York, NY)
- …initiatives. Build scientific platforms alongside our Chief Scientific Operations Officer, Senior Director , and Lead Principal Scientist . Define a Medical ... the organization. Cross-functional Collaboration: Work closely with clinical development, regulatory affairs, market access, and commercial teams to align strategies… more
- Organon & Co. (Jersey City, NJ)
- **Job Description** **The Position** The Principal Scientist ( Director ) Regulatory CMC is responsible for Regulatory Chemistry Manufacturing & ... management for the assigned portfolio of small molecule or biologic products. The Principal Scientist may also support project team goals and organizational… more
- Merck (Rahway, NJ)
- … Principal Scientist , CMC, R4 - Pharm Pre-approval Reporting to the Sr Director / Director / Principal Scientist /Sr Principal Scientist in ... Pharmaceutical CMC is responsible for developing and implementing CMC regulatory strategies for our company's pharmaceutical pipeline products in accordance… more
- Organon & Co. (Jersey City, NJ)
- …**The Position** The Associate Principal Scientist (Associate Director ) is responsible for developing and implementing Regulatory Chemistry, ... in accordance with global regulations and guidances, and Organon procedures. The Associate Principal Scientist will lead the preparation and submission of CMC… more
- Merck (Rahway, NJ)
- …Summary** + Under the guidance of a senior leader, an Associate Principal Scientist /Associate Director , has primary responsibility for planning/managing ... 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)
- **Job Description** **Role Summary** + The Principal Scientist / Director , Value & Implementation (V&I) Outcomes Research, position resides in the V&I ... 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)
- …Description** **Role Summary** + Under the guidance of an Executive Director , has primary responsibility for developing value evidence strategies, and ... 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)
- **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)
- …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)
- …process validation, second generation process development and authoring of regulatory submissions. Under the general scientific and administrative direction of ... the Director in Biologics Cell Culture Sciences group and working...next generation process development and characterization, process validation, and regulatory submission authoring **In this role, the successful candidate… 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
