长沙招聘

工作职责:

1. Be responsible for clinical trial non-drug supplies management including order，tracking，shipment，retrieval and destrution.

2. Be responsible for Trial Master File(FMF) management including binder set up.

3. Be responsible for study Finance management.

4. Support CPL on Clinical Trial related administravtive works assigned by line manager.

5. Be responsible for study file archiving (CCO only).

任职资格:

1. College degree or equivalent or above,major in medicine/pharmacy/scinece related is preferred.

2. Experience in Clinical Research/Development 0r related industry(appreciated).

3. GCP/GMP knowiedge on clinical supply management.

泰格医药是行业领先的一体化生物医药研发服务平台，为全球制药和医疗器械行业提供跨越全周期的临床研究创新解决方案。通过全面的服务体系和***的质量标准，我们助力生物医药产业提升研发效率、降低研发风险，确保研究项目高质量交付，加速医药产品市场化进程，履行对行业和患者的承诺。同时，我们也通过覆盖各领域的80多家子公司，打造赋能全产业链的创新生态，推动医疗产业创新和发展。作为全球化的研发平台，泰格医药在全球布局170多个办事处和研发基地，拥有超过8600人的专业团队，覆盖5大洲的51个国家，致力于解决最具挑战的全球健康问题，满足患者的未尽医疗需求，创造社会价值，造福人类健康。