- Merck (Boston, MA)
- **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 (Boston, MA)
- **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 (Boston, MA)
- …talented and dedicated colleagues while developing and expanding your career. The Senior Director (Sr. Principal Scientist ) has primary responsibility for ... of clinical development, including study design, placement, monitoring, analysis, regulatory reporting, and publication. **Specifically, The Senior Director … more
- Regeneron Pharmaceuticals (Cambridge, MA)
- Job Description We are looking for a highly motivated Principal Scientist , Clinical Pharmacology in our Pharmacometrics (PMx) group. The position will report to ... the Senior Group Director (SGD) within Clinical Pharmacology (CP) in the General...into clinical study reports + Provide CP support of regulatory documents, communications, and presentations (eg, IND, health authority… more
- Novo Nordisk (Lexington, MA)
- …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 (Boston, MA)
- …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 (Cambridge, MA)
- …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 (Cambridge, MA)
- …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
- Fenway Health (Boston, MA)
- …approval and assistance of the site Principal Investigator or research scientist , ensuring adherence to ethical and regulatory standards. + Meeting ... Communication:Regularly communicate initiatives, progress, and updates to the Project Director and Principal Investigator, ensuring transparency and alignment… more