- Merck & Co. (Rahway, NJ)
- …studiesWork closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical ... with talented and dedicated colleagues while developing and expanding your career.The Senior Director (Sr. Principal Scientist ) has primary responsibility for… more
- Merck & Co. (Rahway, NJ)
- …studies;Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical ... dedicated colleagues while developing and expanding your career.--The Director (Principal Scientist ) has primary responsibility for the planning and directing of… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …including working with contract manufacturing organizations CMO. This position serves as the Regulatory Affairs (RA) CMC project representative to the CMC sub ... applications/supplements & variations (eg, NDA, BLA, MAA). This position authors regulatory documents where necessary with supervision. This position conducts … more
- Merck & Co. (Rahway, NJ)
- …Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development ... Job DescriptionThe Senior Clinical Director (Sr. Principal Scientist )...pursue and subsequent study design, initiation, execution, monitoring, analysis, regulatory filing, and publication. Specifically, The Senior … more
- Organon & Co. (Jersey City, NJ)
- …to the Director in Regulatory Chemistry, Manufacturing and Controls, the Senior Scientist is responsible for implementing Regulatory Chemistry, ... products in accordance with global regulations, guidance's and defined regulatory strategies. The Senior Scientist is responsible for the preparation and… more
- Merck (Rahway, NJ)
- …product withdrawal. + Support new technology development. + Demonstrate an understanding of regulatory affairs and applies this understanding to the benefit of ... **Job Description** Under general supervision of an Executive Director/ Senior Director, the Principal Scientist /Director is responsible for developing and… more
- Merck (Rahway, NJ)
- …+ Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development ... talented and dedicated colleagues while developing and expanding your career. The Senior Director ( Senior Principal Scientist ) has primary responsibility… more
- Merck (Rahway, NJ)
- …create breakthrough science changing the way we approach animal health challenges. The Senior Scientist within our company's Animal Health Formulation Group is ... interfacing with other functional areas (eg project management, manufacturing, quality, regulatory affairs ) and external partners to drive project milestones… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …including working with contract manufacturing organizations CMO.** This position serves as the Regulatory Affairs (RA) CMC project representative to the CMC sub ... applications/supplements & variations (eg, NDA, BLA, MAA). This position authors regulatory documents where necessary with supervision. This position conducts … more
- Merck (Rahway, NJ)
- …scientists (including discovery research, biostatistics, drug metabolism, modeling and simulation, regulatory affairs , and global clinical trials operations) + ... Translational Medicine Operations, Translational Medicine-EU, Drug Metabolism/Modeling & Simulation, Regulatory Affairs , and late-stage Clinical Research throughout… more
- Merck (Rahway, NJ)
- …+ Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development ... colleagues while developing and expanding your career. The Director (Principal Scientist ) has primary responsibility for the planning and directing of clinical… more
- Merck (Rahway, NJ)
- **Job Description** Under the guidance of a senior leader, the Principal Scientist , Outcomes Research-Women's Cancer has primary responsibility for developing ... incumbent is expected to work cross-functionally with clinical development, medical affairs , biostatistics, market access, commercial and country affiliates and may… more
- City of New York (New York, NY)
- …where they are from or where they live. Position Summary: BHHS's Policy and External Affairs Program seeks a Senior Policy Advisor to lead its health systems ... and Treatment, HIV Epidemiology, HIV Prevention, Policy and External Affairs , Racial Equity and Social Justice Initiatives, STI, and...STI, and viral hepatitis policy advocacy more broadly. The Senior Policy Advisor will report to the Director of… more
- Merck (Rahway, NJ)
- …Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development ... **Job Description** The ** Senior Clinical Director (Sr. Principal Scientist )**...pursue and subsequent study design, initiation, execution, monitoring, analysis, regulatory filing, and publication. **Specifically, The Senior … more
- Regeneron Pharmaceuticals (Basking Ridge, NJ)
- The Senior Medical Director, Clinical Sciences, Hematology provides clinical leadership and is responsible for all clinical deliverables within the assigned section ... with the Clinical Development Plans (CDP); clinical components of regulatory documents/registration dossier and brand related medical information, clinical… more
