- Merck & Co. (North Wales, PA)
- Job DescriptionThe Regulatory Affairs Headquarters Principal Scientist is responsible for development and implementation of global regulatory strategy ... regulatory point of contact on those projects within Global Regulatory Affairs and Clinical Safety (GRACS) and external to GRACS.Develops worldwide product … more
- Merck & Co. (North Wales, PA)
- …divestment and product withdrawal.Support new technology development.Demonstrate an understanding of regulatory affairs and applies this understanding to the ... general supervision of an Executive Director/Senior Director, the Principal Scientist /Director is responsible for developing and implementing Chemistry,… more
- Merck & Co. (South San Francisco, CA)
- …(including discovery research, biostatistics, drug metabolism, modeling and simulation, regulatory affairs , and global clinical trials operations).Provide ... Translational Medicine Operations, Translational Medicine-EU, Drug Metabolism/Modeling & Simulation, Regulatory Affairs , and late-stage Clinical Research throughout… more
- Merck & Co. (Rahway, NJ)
- …studiesWork closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical ... while developing and expanding your career.The Senior Director (Sr. Principal Scientist ) has primary responsibility for the planning and directing clinical research… more
- Merck & Co. (North Wales, PA)
- Job DescriptionUnder the guidance of a senior leader, the Principal Scientist , Outcomes Research-Women's Cancer has primary responsibility for developing value ... incumbent is expected to work cross-functionally with clinical development, medical affairs , biostatistics, market access, commercial and country affiliates and may… 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)
- …and validation, collaborating with project teams, biomarker leaders, clinical operations and regulatory affairs on the implementation of these assays in clinical ... in support of clinical trials. The candidate for this Associate Principal Scientist position should have strong technical expertise in Liquid Chromatography and Mass… more
- Merck & Co. (Boston, MA)
- …scientists (including discovery research, biostatistics, drug metabolism, modeling and simulation, regulatory affairs , and global clinical trials operations) for ... Job DescriptionWe have an exciting opportunity for a physician- scientist to join our group as a- Principal Scientist (Clinical Director) in Translational… 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 ) has primary responsibility for the strategic planning and directing clinical research… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …Hub. Key internal stakeholders include Medical & Science, Clinical Operations, Regulatory Affairs , Data Management, Biostatistics, Non-clinical, Medical ... Global Safety Lead(s), Global Safety Lead(s) and Global Safety Scientist (s)/Associate within Safety Surveillance. Essential Functions Innovation and change… more
- Organon & Co. (Jersey City, NJ)
- **Job Description** **The Position** Reporting to the Director in Regulatory Chemistry, Manufacturing and Controls, the Senior Scientist is responsible for ... assigned biological products in accordance with global regulations, guidance's and defined regulatory strategies. The Senior Scientist is responsible for the… more
- Organon & Co. (Plymouth Meeting, PA)
- … Chemistry, Manufacturing and Controls New Products, the Associate Principal Scientist (Associate Director) is responsible for Regulatory Chemistry, ... molecule products in accordance with global regulations, guidance's and defined regulatory strategies. These products may be internal or acquired or licensed… more
- Organon & Co. (Plymouth Meeting, PA)
- …**The Position** Reporting to the Director or Executive Director in Organon Regulatory CMC New Products, the Associate Principal Scientist (Associate Director) ... development products and commercially approved compounds. The Associate Principal Scientist may also support project team goals and organizational initiatives,… more
- Merck (Philadelphia, PA)
- **Job Description** The Regulatory Affairs Headquarters Principal Scientist is responsible for development and implementation of global regulatory ... global regulatory point of contact on those projects within Global Regulatory Affairs and Clinical Safety (GRACS) and external to GRACS. + Develops worldwide… more
- Lilly (Indianapolis, IN)
- …support for Clinical Trial Applications, Market Registrations And Post-Approval Submissions. The Research Scientist in Global Regulatory Affairs - CMC will ... world. We are seeking an Advisor/Senior Advisor for Global Regulatory Affairs CMC to be a part...CMC strategies and develop submissions for marketing authorizations. The Regulatory Scientist is expected to develop and… more
- Lilly (Indianapolis, IN)
- …operational support for market registrations and post-approval submissions. The regulatory scientist in Global Regulatory Affairs - CMC Biotechnology ... new medicines to patients who need them all over the world. We are seeking Regulatory Scientist GRA-CMC to be a part of the Lilly global regulatory group to… more
- ADM (Decatur, IL)
- …Nutrition - Decatur, IL **Department/Function:** Legal, Compliance, Regulatory Affairs , Corporate Security **Job Description:** **Senior Scientist Human ... to protect and enable business growth. + Partner with Regulatory Affairs to develop and deploy global...5+ years for Scientist ; 15+ for Sr. Scientist . + Experience with regulatory approval of… more
- AbbVie (North Chicago, IL)
- …Process Engineering, Drug Product Development, and Quality Assurance and Regulatory Affairs . + Serve as the lead analytical scientist on the development ... LinkedIn. Job Description We are seeking a highly motivated, experienced analytical scientist to impact early phase development of New Chemical Entities (NCEs) in… more
- Lilly (Indianapolis, IN)
- …discovery + Drug/clinical development experience (for example, epidemiology, toxicology, pharmacology, regulatory affairs , medical affairs ) If experience is ... make life better for people around the world. **Clinical Research Scientist - Medical Affairs ** Through the application of scientific and clinical training and… more
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