Assistant Manager, Clinical Pharmacology - 2026 Global Talent Program

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. Qualifications Education: Ph.D. in Clinical Pharmacology, Pharmaceutical Sciences, or a directly related scientific field. Required Skills Proactive Execution: Demonstrated ability to independently drive projects to completion efficiently and effectively. Critical Thinking: Strong capabilities in independent research, complex problem-solving, logical analysis, and scientific literature evaluation. Effective Communication: Excellent verbal and written communication skills for clear, concise dialogue with internal and external stakeholders. Collaboration & Teamwork: Proven ability to collaborate effectively within cross-functional teams and build strong working relationships. Resilience & Adaptability: Capacity to thrive in a dynamic, fast-paced environment, managing competing priorities and meeting deadlines under pressure. #J-18808-Ljbffr Hengrui Pharma