长沙招聘

工作职责:

工作职责：This position provides statistical support to development and clinical research projects; interacts with research personnel to ascertain needs and develops appropriate design and statistical solutions. Develops/Coordinates statistical analysis plans (SAPs) and statistical reports for use by internal and external customers. Monitors work to ensure quality, and continuously promote Quality First Time and ensures compliance with the company SOPs, Policies, Directives, Divisional standards, Declaration of Helsinki, Industry standards, relevant GxPs, both CNMPA and/or international requirements and/or best practices.

1. Interact with product developers and clinical investigators to design clinical trials with appropriate statistical methods and adequate sample size for statistical justification of clinical utility claims.

2. Write data analysis plans as needed to capture design elements and statistical methodology.

3. Perform/Support data analysis and prepares statistical reports of results.

4. Perform Quality Control (QC) for statistical analyses to ensure analysis quality.

5. Conduct randomization and blinding of samples, if apply.

6. Maintain expertise in state-of-the-art data manipulation and statistical analyses.

7. Manage technical aspects of project(s), as assigned.

8. Monitor work to ensure quality, and continuously promotes Quality First Time.

9. If apply, be a contact window, develop and maintain a good working relationship with BAs and other dept. to support the cross-functional projects

10. Other projects or tasks assigned by line manager

11. Conduct business in full compliance including but not limited to Roche Secure, Roche Behavior in Business, Roche Competition Law Interactive Dialogues, Roche Safety, Security Health and Environmental Protection

任职资格:

1. At least Master degree in Statistics or a related field, at least 2 years of relevant experience

2. Proficiency in English language skills

3. Good command of SAS or other statistical software

4. Understand pharmaceutical and/or medical device regulation and ICH/GCP

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。