- Merck (North Wales, PA)
- **Job Description** Under the guidance of a senior leader, the Principal Scientist ( Director ), Outcomes Research-Women's Cancer will be a member of the ... healthcare resource utilization and costs, physician and patient satisfaction surveys, clinical and patient reported outcomes assessments, and systematic reviews and… more
- Merck (Rahway, NJ)
- **Job Description** **Device Development Associate Principal Scientist - Development Strategy, Design Controls** **(Associate Director Equivalent)** _Our ... development and design control principles to positively support and influence clinical and commercial combination product development and launches to ensure they… 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 (Rahway, NJ)
- …final regulatory review and approval of: + Worldwide marketing applications + Clinical study protocols and reports + Investigator brochures + Local registration ... Conduct initial content review and approval for IND/CSA submissions to enable clinical trial initiation. + Participate in regulatory due diligence activities for… more
- Merck (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… 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