- Merck (Rahway, NJ)
- **Job Description** **Title: Associate Principal Scientist /Associate Director , Outcomes Research** **Role Summary** + Under the guidance of a senior leader, ... an Associate Principal Scientist /Associate Director , has primary...reimbursement and market access, and provide input into clinical, regulatory , payer/access, marketing and evidence generation strategy and programs… more
- Merck (Rahway, NJ)
- …ensure products and processes are developed in accordance with applicable regulatory , quality, company, and customer requirements. This position will lead ... and influence clinical and commercial combination product development and launches. ** Principal Responsibilities** + Lead and set direction for the device… more
- Merck (Rahway, NJ)
- **Job Description** We have an exciting opportunity for a ** Principal Scientist ( Director ) in Translational Medicine** . Translational Medicine at our ... Clinical Research while developing and expanding your career. **Primary responsibilities for the Principal Scientist include the following:** + Key member of an… more
- Merck (Rahway, NJ)
- …talented and dedicated colleagues while developing and expanding your career. The Senior Director (Senior Principal Scientist ) has primary responsibility for ... of clinical development, including study design, placement, monitoring, analysis, regulatory reporting, and publication. **Specifically, The Senior Director … more
- Merck (Rahway, NJ)
- **Job Description** The **Clinical Director ( Principal Scientist )** has primary responsibility for the strategic planning and directing clinical research ... to pursue and subsequent study design, initiation, execution, monitoring, analysis, regulatory filing, and publication. **Specifically, The Clinical Director May… more
- Merck (Rahway, NJ)
- …of our company's Research Laboratories Division is seeking applicants for a Principal Scientist position available at our company's research facility. The ... Principal Scientist is a senior scientific role tasked with working closely with the group Director to define group strategy and to lead a team of scientists… more
- Bristol Myers Squibb (New Brunswick, NJ)
- …their personal lives. Read more: careers.bms.com/working-with-us . **Position Summary** The Principal Process Engineer/ Scientist acts as a technology transfer ... applicable cGMPs, BMS procedures, and that processes are defined consistent with regulatory filings. This position will also work on new technology initiatives for… more
- WuXi AppTec (Plainsboro, NJ)
- **Overview** With supervision serve as study director / principal investigator to perform MD, MV/MQ and Sample analysis for Large Molecule (LM) Bioanalysis ... subordinates and/or less experienced staff. + Assists in training Associate Scientist . + Laboratory Maintenance + Follows company's safety policies, practices and… more
- Novo Nordisk (Plainsboro, NJ)
- …late-stage clinical development. We are building a multi-talented team of physician scientist drug developers that works together to tackle key challenges and ... living. Are you ready to make a difference? The Position The International Medical Director serves as a subject matter expert for our products and related data… more
- Merck (Rahway, NJ)
- …and dedicated colleagues while developing and expanding your career. **The Senior Director (Senior Principal Scientist )** has primary responsibility for ... of clinical development, including study design, placement, monitoring, analysis, regulatory reporting, and publication. **Specifically, the Senior Director … more
- Bristol Myers Squibb (Princeton, NJ)
- …at work and in their personal lives. Read more: careers.bms.com/working-with-us . Senior Principal Scientist - DMPK Project Representative When you join BMS, you ... the globe. PCO "is looking for a Scientific Associate Director to join the Dev DMPK group that is...activities of multiple projects; be responsible for preparation of regulatory dossier/responses; and assist in developing strategy for the… more
- Bristol Myers Squibb (Princeton, NJ)
- …and acting on clinical trial data to support development + Serving as principal functional author for Regulatory submission, study reports, and publications + ... lifecycle + Manages site interactions in partnership with the Clinical Scientist for medical questions and education (including safety management guidelines) +… more