Senior Manager, Clinical Pharmacology & DMPK

Role: Senior Manager, Clinical Pharmacology & DMPK, overseeing clinical pharmacology, PK, DM, and bioanalytical functions for Summit's oncology assets, including late-stage NSCLC and colorectal cancer trials. Responsibilities: manage PK/ADA sample collection, processing, storage, and vendor relationships; design and oversee in vitro/in vivo ADME studies; ensure data integrity and GCP compliance; perform data analysis and reporting; collaborate cross-functionally on sample logistics and study design. Requirements: Ph.D. or Pharm.D. in pharmacokinetics, pharmaceutical sciences, or related discipline; 1+ years (Ph.D.) or 5+ years (M.S.) industry experience in clinical pharmacology; knowledge of regulatory guidelines (GCP, ICH); proficiency with PK software (e.g., Phoenix WinNonlin); strong project management and communication skills. HighValue: focus on oncology (NSCLC, CRC), late-stage (Phase 3) clinical studies, bioanalytical and DMPK expertise, regulatory compliance, cross-functional collaboration, vendor management. WorkSetup: not specified; likely corporate setting.