- 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 (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 (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