Assistant Manager, Clinical Pharmacology - 2026 Global Talent Program

Responsibilities

• Research & Planning: Conduct comprehensive research and synthesize clinical pharmacology and clinical trial data for assigned products; contribute to the development of Clinical Pharmacology Development Plans.
• Document Authoring: Draft high-quality clinical pharmacology study documents, including protocols and Clinical Study Reports (CSRs).
• Data Analysis & Interpretation: Analyze and interpret data generated from clinical pharmacology trials to inform development strategies.
• Study Start-up Support: Coordinate and prepare essential documentation for clinical research site initiation and ethics committee submissions.
• Regulatory Coordination: Manage clinical trial registration and associated regulatory filings.
• Trial Execution: Participate actively in the implementation, oversight, and progress of clinical pharmacology studies.

Qu...