- 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)
- …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 (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 (North Wales, PA)
- …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 (Upper Gwynedd, PA)
- **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 (North Wales, PA)
- …with talented and dedicated colleagues while developing and expanding your career. The Director ( Principal Scientist ) has primary responsibility for the ... cycle of clinical development, including study design, placement, monitoring, analysis, regulatory reporting, and publication. **Specifically, the Director may… more
- Merck (West Point, PA)
- …we collaborate to discover the next medical breakthrough. We are seeking a Principal Scientist to join our Vaccine Analytical Research and Development team ... West Point, PA. In this role, an individual will work closely with the group Director to define group strategy and lead a team of scientists in solving complex… 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
- Merck (North Wales, PA)
- …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