长沙招聘

工作职责:

1. Reviewing and implementing Global and regional Procedural Documents.

2. Developing, implementing and maintaining local Procedural Documents and processes.

3. Delivering training to the department to emphasize the procedural key points and the update according to GCP, relevant SOPs and QC manuals.

4. Assuring China MA Evidence Generation is ready for audit and inspection at any time.

5. Conducting quality control checks in clinical trials as agreed with Global/regional and local clinical study

team leaders.

任职资格:

-Academic / Professional qualification

? Bachelor degree or above of medical/pharmaceutical specialty

? Proven experience of the execution of clinical studies or pharmacovigilance

-Technical / skill training

? Strong interpersonal skills, with the ability to work effectively with stakeholders at all levels

? Excellent competence of GCP/GVP and clinical study procedure or pharmacovigilance

? Good presentation skills

? Proven ability to deliver training

? Familiar with budgeting

-Working experience

? 3-year working experience in relevant for a multinational pharmaceutical company.

Study- working experience as a CRA and Clinical management staff for studies

PV – working experience as PV physician or PV specialist.

? At least 1-2 years as Associate QC Mgr. or equivalent.

? 1-2 years proven training or coaching experience.

? Procedural documents generating experience.

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。