长沙招聘

职位描述：
Responsibilities：
（1）Distribute completed documents to sites and internal project team members.
（2）Prepare site regulatory documents, reviewing for completeness and accuracy.
（3）Review, prepare and negotiate site contracts and budgets with sites.
（4）Ensure accurate completion and maintenance of internal systems, databases and tracking tools with project specific information.
（5）Review and provide feedback to management on site performance metrics.
（6）Inform team members of completion of regulatory and contractual documents for individual sites.
（7）Review, track and follow up the progress, the approval and execution of documents, including contracts, regulatory, ethics ICF and IP Release documents, in line with project timelines.
（8）Provide local expertise to SSU leads and Project team.

Working Experience ：
（1）1 year‘s clinical research or other relevant experience; or equivalent combination of education, training and experience.
（2）Experience of CRA experiences (preferred).
Language ability ：
（1）Good command of written and verbal English. 举报 分享

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。