
中层管理(经理/总监)
AI 估算 · 25k–40k
临床研究管理职位,经验要求高,市场竞争力中等偏上,参考上海北京CRO经理薪资。
该职位是精鼎医药(Parexel)的临床医生/临床经理,负责为临床试验提供科学和临床专业支持,包括制定试验策略、撰写方案和修正案、培训研究团队、与研究者沟通等
Key Accountabilities: General Accountabilities Provides clinical and scientific expertise to the clinical trial strategy and protocol development process, including acquisition of knowledge of competitor products. Designs/writes clinical trial outlines, protocols and amendments, in collaboration with internal contributors and external experts. Creates clinical/protocol training materials. Helps establish and oversees Data Monitoring Committees (DMCs) and endpoint adjudication committees. Maintains direct contact with investigative sites. Compliance with Parexel standards: Complete timesheets, submit expense reports, update CV, maintain working knowledge of ICH-GCPs and other requirements. Strong Communication Skills. Demonstrated project management / leadership experience. Knowledge and Experience: Preferred: Thorough understanding of local / international regulations applicable to clinical trials. Practical experience in clinical trial strategies, methods and processes. Track record of design, oversight and interpretation of clinical studies. Previous leadership /management experience or training. Knowledge and experience in Good Clinical Practices. Fluent in both oral and written English. Fluent in host country language required. Education: Fluent in host country language required.
Key Accountabilities: General Accountabilities Provides clinical and scientific expertise to the clinical trial strategy and protocol development process, including acquisition of knowledge of competitor products. Designs/writes clinical trial outlines, protocols and amendments, in collaboration with internal contributors and external experts. Creates clinical/protocol training materials. Helps establish and oversees Data Monitoring Committees (DMCs) and endpoint adjudication committees. Maintains direct contact with investigative sites. Compliance with Parexel standards: Complete required training curriculum, timesheets, expense reports, update CV, maintain working knowledge of ICH-GCPs and other applicable requirements.
优点
缺点 / 挑战
暂无明显挑战项
跨国CRO临床医生/经理,专业成长空间大,薪资中等,但工作强度较高且需现场办公。
职位未明确提及薪资福利,但CRO行业薪资水平中等偏上,稳定性较好,补偿性动机满足程度一般。
职位提供丰富的临床研究全流程经验,涉及策略制定和领导机会,发展性动机满足度高。
仅现场办公,且可能涉及出差,工作强度较大,生活化动机满足度较低。
参与新药研发,改善患者健康,社会价值高,行业前景好,意义感动机满足度高。