- Merck & Co. (Rahway, NJ)
- …with talented and dedicated colleagues while developing and expanding your career.The Senior Director ( Sr . Principal Scientist ) has primary responsibility ... studiesWork closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical… more
- 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)
- …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. (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.--The Director (Principal Scientist ) has primary responsibility for the planning and directing of… 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
- Kelly Services (Clark, NJ)
- …individuals in the marketplace. We are proud to offer an opportunity to work as a ** Sr Scientist , Regulatory Affairs ** located in Clark, NJ. **Duration** ... **Compensation** : $50-60/hr **Purpose of the Role: ** 1. Administer regulatory affairs over the product lifecycle from pre-market concept, product development,… more
- Mondelez International (East Hanover, NJ)
- …to Lead the Future of Snacking. Make It With Pride.** The Sr . Scientist II will execute the Scientific Affairs Strategy for your respective categories and ... process may contact ### for assistance. **Job Type** Regular Scientific Affairs & Regulatory Affairs Product Quality, Safety and Compliance At Mondelēz… more
- Pfizer (New York, NY)
- **ROLE SUMMARY** The Clinical Scientist (CS) - Sr . Manager will support clinical epidemiology study execution for multiple studies for one or more vaccine ... programs. In collaboration with Scientific Affairs (SA) / Clinical Epidemiology, Biostatistics group and Clinical Affairs (CA) Operations, the CS is responsible… more
- Haleon (Warren, NJ)
- …to be part of something special. **About the Role** As a ** Senior Scientist - Medical & Scientific Affairs ** , you will be responsible for providing ... related field. + 2+ years of experience in Medical Affairs , R&D, Regulatory Affairs within...on the achievement of key business performance and other incentive/ recognition programs as part of the offering. The salary… more
- Pfizer (New York, NY)
- …CMAO, Medical Affairs Strategy, Biostatistics & Data Management, Global Regulatory Affairs , Clinical Pharmacology / Pharmacometrics, Market Access, Business ... **ROLE SUMMARY** **The Platform:** The Chief Medical Affairs Office's Real World Evidence (RWE) Platform is...needed and warranted as a hybrid strategic lead and scientist . To carry out this work, they will be… more
- Merck (Rahway, NJ)
- …with talented and dedicated colleagues while developing and expanding your career. The Senior Director ( Sr . Principal Scientist ) has primary responsibility ... + Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development… 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
- 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
- Haleon (Warren, NJ)
- …of something special. **About the role:** The US Medical and Science Innovation Senior Scientist is accountable for providing medical and scientific expertise to ... required. Ideally will have experience in and/or working with Medical or Regulatory Affairs , Clinical Research/Development, and/or Innovation. + The role… 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
- Regeneron Pharmaceuticals (Basking Ridge, NJ)
- …looks like:** + Partners with the CDSL Managers, the Formulation Development Group (FDG), Regulatory Sciences (RS)/ Affairs (RA), as well as members of the ... The Senior Manager, Pharmacy Support Lead (PSL) is responsible...Study Lead (CSL), Study Medical Director (SMD) and Clinical Scientist (CS), Quality Management Lead (QML **).** + Provides… 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