- Merck (Trenton, NJ)
- **Job Description** As the Director / Principal Scientist in Devices and Drug-Device Combinations CMC (Chemistry, Manufacturing & Controls), you will report to ... the Director of Device Regulatory Affairs for Autoinjector Development Programs. You will spearhead regulatory activities for Devices and Drug-Device… more
- Merck (West Point, PA)
- **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 (West Point, PA)
- **Job Description** **Job Title:** **Associate Principal Scientist , Cell Culture and Fermentation Sciences Level: R4 (Research Path)** **Level:** **P4 (Research ... manufacturing sites, manufacturing investigations, process validation, and authoring of regulatory submissions. Under the general scientific and administrative direction… 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
- 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