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Key Responsibilities :
- Research and compile product-related clinical pharmacology and clinical trial information; participate in developing clinical pharmacology R&D plans;
- Draft clinical pharmacology-related trial documents (e.g., protocols, CSRs);
- Analyse and process data generated from clinical pharmacology trials;
- Coordinate and prepare materials for clinical research site initiation and ethics approval;
- Complete clinical trial registration and filing-related tasks;
- Participate in the implementation and advancement of clinical pharmacology trials.
Qualifications : Education :
PhD or higher in Clinical Pharmacology or related field
Language Requirements :
Proficient in reading, communication, and writing in both Chinese and English
Other Skills : Proficient with office software
Competency Requirements :
Strong execution abilityStrong independent research and logical thinking skillsClear written and oral communication skillsStrong team spirit and good collaboration skillsgood literature search abilityGood adaptability, able to work under time constraints and pressureStrong professional ethics