- Merck & Co. (Rahway, NJ)
- …Research and Development (ARD)-at our company's Research Laboratories is seeking a senior scientist to work onsite with extensive experience in validation ... closely with other analytical groups in ARD , Global Quality and Regulatory Affairs -CMC to ensure that validated methods are appropriately transferred from our… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionPosition Description: Senior Scientist - Residual Assays, Analytical R&D We invite individuals who possess a deep passion for promoting lifesaving ... individual to join our Rahway, NJ team as a Senior Scientist (R3) in Biologics Analytical Research...Molecule Assay Validation, Quality Assurance, Technical Operations, and CMC Regulatory Affairs , to address technical challenges,… more
- 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
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …with cross functional teams and various departments to include Marketing, Medical Affairs , Regulatory Affairs , Supply Chain Technical Operations, ... The Associate Director, RACMC Portfolio Products, will be responsible for regulatory CMC (Chemistry, Manufacturing, and Controls) activities of the portfolio small… 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)
- …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.-- Director (Principal Scientist ) has primary responsibility for the planning and directing of… 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
- Merck & Co. (Rahway, NJ)
- …may:Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development ... Job DescriptionThe Clinical Director (Principal Scientist ) has primary responsibility for planning and directing clinical research activities involving… more
- Organon & Co. (Jersey City, NJ)
- …Chemistry, Manufacturing and Controls (CMC) New Products, the Senior Scientist is responsible for implementing Regulatory Chemistry, Manufacturing & Controls ... products including biosimilars in accordance with global regulations, guidances and defined regulatory strategies. The Senior Scientist is responsible for… more
- Merck (Rahway, NJ)
- **Job Description** **Position Description:** ** Senior Scientist - Residual Assays, Analytical R&D** We invite individuals who possess a deep passion for ... individual to join our Rahway, NJ team as a Senior Scientist (R3) in Biologics Analytical Research...Molecule Assay Validation, Quality Assurance, Technical Operations, and CMC Regulatory Affairs , to address technical challenges, provide… 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 (Sr. Principal Scientist ) has primary responsibility for the… more
- Merck (Rahway, NJ)
- …Research and Development (ARD) at our company's Research Laboratories is seeking a senior scientist to work onsite with extensive experience in validation & ... closely with other analytical groups in ARD , Global Quality and Regulatory Affairs -CMC to ensure that validated methods are appropriately transferred from our… more
- Pfizer (New York, NY)
- …as appropriate working with Clinical Affairs Lead, Medical/Scientific Affairs Lead and Partner representatives. + Influences management/ senior management ... **ROLE SUMMARY** The Clinician, Clinical Scientist (CS) will provide leadership in clinical epidemiological...at relevant team, governance, external consultants, KOL and potentially regulatory meetings. + Represents Vaccine Clinical Affairs … more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …with cross functional teams and various departments to include Marketing, Medical Affairs , Regulatory Affairs , Supply Chain Technical Operations, ... The Associate Director, RACMC Portfolio Products, will be responsible for regulatory CMC (Chemistry, Manufacturing, and Controls) activities of the portfolio small… 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)
- …+ Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development ... dedicated colleagues while developing and expanding your career. Director (Principal Scientist ) has primary responsibility for the planning and directing of clinical… 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
- City of New York (New York, NY)
- …health and safety of New Yorkers. Reporting to the Chief of Staff, the Senior Science and Policy Advisor will work closely with the Commissioner, colleagues in the ... health agenda through scholarship and other forms of thought leadership. The Senior Science and Policy Advisor will gather, analyze, and summarize key scientific… more
- Regeneron Pharmaceuticals (Tarrytown, NY)
- 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
