- Merck & Co. (Rahway, NJ)
- Job DescriptionDevice Development Associate Principal Scientist - Development Strategy, Design Controls(Associate Director Equivalent) Our company's Device ... development and design control principles to positively support and influence clinical and commercial combination product development and launches to ensure they… more
- Merck & Co. (Rahway, NJ)
- …clinical to post-licensure). With a focus on late-stage development, the Senior Director will manage the entire cycle of clinical development, including study ... and will interact externally with key opinion leaders. Specifically, the Senior Director May Be Responsible For: Evaluating pre- clinical and translational work… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Director ( Principal Scientist ) has primary responsibility for the planning and directing of clinical research activities involving new ... Oncology medicines span all phases of clinical development (pre- clinical to post-licensure). The Director will manage the entire cycle of clinical … more
- Merck & Co. (Rahway, NJ)
- Job DescriptionJoin Our Team as an Associate Principal Scientist /Associate Director in Biologics Drug Substance Commercialization!Are you ready to make a ... in and/or spearhead cross-divisional technical teams focused on late-stage clinical process development, characterization, and technology transfer of biopharmaceutical… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionRole SummaryUnder the guidance of a senior leader, an Associate Principal Scientist /Associate Director , has primary responsibility for ... resource utilization and costs, physician and patient satisfaction surveys, clinical and patient reported outcomes assessments, systematic reviews and meta-analyses,… more
- Merck & Co. (North Wales, PA)
- Job DescriptionRole SummaryThe Principal Scientist / Director , Value & Implementation (V&I) Outcomes Research, position resides in the V&I organization, which ... resource utilization and costs, physician and patient satisfaction surveys, clinical and patient- reported outcomes assessments, systematic reviews and… more
- Merck & Co. (Rahway, NJ)
- …of our Company's Research & Development Division is seeking applicants for a Principal Scientist position available at its Rahway, New Jersey 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… more
- Bristol Myers Squibb (Princeton, NJ)
- …track record of high-quality scientific publications in relevant fields For the Sr. Principal Scientist position, the starting compensation for this job is a ... the transition of drug candidates from early to late-stage clinical development, their approval and life cycle management. Early-stage...+ Minimum of 6 years post-PhD experience for Sr. Principal Level (and minimum of 8 years Post-PhD experience… more
- Merck (North Wales, PA)
- **Job Description** **Role Summary** + The Principal Scientist / Director , Value & Implementation (V&I) Outcomes Research, position resides in the V&I ... resource utilization and costs, physician and patient satisfaction surveys, clinical and patient- reported outcomes assessments, systematic reviews and… more
- Merck (Rahway, NJ)
- …Summary** + Under the guidance of a senior leader, an Associate Principal Scientist /Associate Director , has primary responsibility for planning/managing ... resource utilization and costs, physician and patient satisfaction surveys, clinical and patient reported outcomes assessments, systematic reviews and meta-analyses,… more
- Merck (Rahway, NJ)
- **Job Description** Join Our Team as an Associate Principal Scientist /Associate Director in Biologics Drug Substance Commercialization! Are you ready to make ... in and/or spearhead cross-divisional technical teams focused on late-stage clinical process development, characterization, and technology transfer of biopharmaceutical… more
- AbbVie (North Chicago, IL)
- …LinkedIn and Tik Tok (https://www.tiktok.com/@abbvie) . Job Description Purpose: The Senior Principal Research Scientist / Director of Drug Metabolism and ... in designing and executing biotransformation studies, including both nonclinical and clinical studies. + Develop and implement strategic plans for drug metabolism… more
- Merck (Rahway, NJ)
- **Job Description** The Director ( Principal Scientist ) has primary responsibility for the planning and directing of clinical research activities ... Oncology medicines span all phases of clinical development (pre- clinical to post-licensure). The Director will manage the entire cycle of clinical … more
- Merck (North Wales, PA)
- …Description** **Role Summary** + Under the guidance of an Executive Director , has primary responsibility for developing value evidence strategies, and ... resource utilization and costs, physician and patient satisfaction surveys, clinical and patient reported outcomes assessments, systematic reviews and meta-analyses,… more
- Merck (West Point, PA)
- …and/or spearhead cross-divisional technical teams focused on late-stage clinical process development, characterization, and technology transfer of biopharmaceutical ... Biochemical Analysis, Biodesign, Biological Engineering, Bioprocessing, Chemical Engineering, Chromatography, Clinical Process, Communication, Data Analysis, Decision Making, Detail-Oriented, Foster… more
- Catalent Pharma Solutions (Baltimore, MD)
- …focus on Quality by Design principles and regulatory compliance. The Principal Scientist will report to the Senior Director of Analytical Development and is ... ** Principal Scientist , Analytical Development** **Summary:** Catalent...Scientist - Analytical Development will report to the Senior Director , Analytical Development. **Catalent is committed to a Patient… more
- Organon & Co. (Plymouth Meeting, PA)
- **Job Description** **The Position** The Associate Principal Scientist (Associate Director ) is responsible for developing and implementing Regulatory ... in accordance with global regulations and guidances, and Organon procedures. The Associate Principal Scientist will lead the preparation and submission of CMC… more
- Takeda Pharmaceuticals (Boston, MA)
- …life-changing therapies to patients worldwide. Join Takeda as a **Senior** ** Principal Pharmacovigilance Scientist ** where you will provide pharmacovigilance ... will contribute:** + Technically fully competent to perform all usual Principal Pharmacovigilance Scientist /Senior Pharmacovigilance Scientist workload,… more
- Organon & Co. (Jersey City, NJ)
- **Job Description** **The Position** The Principal Scientist ( Director ) Regulatory CMC is responsible for Regulatory Chemistry Manufacturing & Controls (CMC) ... aspects of projects in clinical phase through initial product registration and post approval...assigned portfolio of small molecule or biologic products. The Principal Scientist may also support project team… more
- Bristol Myers Squibb (Devens, MA)
- …in their personal lives. Read more: careers.bms.com/working-with-us . **Position Summary** The Principal Scientist is a subject matter expert, project owner and ... investigator supporting commercial biologics manufacturing at Bristol-Myers Squibb Devens. The Principal Scientist will oversee and deliver complex technical… more
