- Organon & Co. (Plymouth Meeting, PA)
- …and/or modeling vendors). The TMED Lead will ensure the scientific and clinical pharmacology components of study protocols are sound, based on the most ... position can be 100% remote in the US** The Director , Translational Medicine and Early Development (TMED) Lead...plan (EDP) will represent an integrated plan that leverages clinical pharmacology principles, such as establishing an… more
- Bristol Myers Squibb (Princeton, NJ)
- …to Phase 2/3 clinical study design and registrational strategy + **Accountable for the** Clinical Pharmacology Plan + ** Lead ** design of clinical ... teams, and regulatory submissions; serves as Clinical Pharmacology subject matter expert + ** Lead and...related field (MS, Ph.D. or PharmD) + For Associate Director level with Ph.D. approximately 5+ years experience with… more
- Merck (West Point, PA)
- …registration packages to support global filings, a strong understanding of clinical pharmacology studies to support intrinsic/extrinsic factors, ability to ... **Job Description** **Position Description:** ** Director , Quantitative Pharmacology and Pharmacometrics Immunology (R5)** The Quantitative Pharmacology and… more
- Merck (West Point, PA)
- …registration packages to support global filings, a strong understanding of clinical pharmacology studies to support intrinsic/extrinsic factors, ability to ... **Job Description** The Quantitative Pharmacology and Pharmacometrics (QP2) Department of our Company's...Company's Research Laboratories is seeking a curious and collaborative Director to support our rapidly expanding ophthalmology pipeline. This… more
- Merck (West Point, PA)
- **Job Description** Therapeutic area Senior Directors in Quantitative Pharmacology and Pharmacometrics (QP2) are responsible for driving integrated end-to-end ... multiple assets moving through near-term late development milestones. The IDVAX Senior Director is responsible for driving the portfolio forward leveraging the full… more
- Takeda Pharmaceuticals (Trenton, NJ)
- …best of my knowledge. **Job Description** **About the role:** **Associate Director , Nonclinical Regulatory Writing and Submission Support,** **_Oncology and Marketed ... enables you to engage in meaningful work? Join us as an _Associate Director - Nonclinical Regulatory Writer_ _and Submission Support_ reporting to the Nonclinical… more
- Merck (West Point, PA)
- …development strategy for novel therapy programs from Preclinical Candidate approval through Clinical Pharmacology testing (Phase 1), and clinical ... investment in clinical development programs. + Development and execution of clinical pharmacology strategies to support later stages of development from… more