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2年经验 -
博士 -
招1人 -
11-09 发布
- 五险一金
- 定期体检
职位描述
职位描述： Job Description:?Work in a high motivated team and very dynamic environment, you will extend your potential to limitless. Position level will base on the individual experience and education background.?Work with clients for preliminary studies selection and preliminary detailed study designs based on compound’s nature, clinical indication, intended clinical trial regime, data from previous studies, and the jurisdiction(s) the sponsor intends to submit.?Scientific monitoring process of projects: RTPM will scientifically monitor all the process starting from lead optimization, pharmacology, DMPK (drug metabolism and pharmacokinetics), CMC, safety assessment (toxicology, pathology, analytical/bioanalytical), all the way through IND/CTA submission.?Coordinate with sponsors and internal expertise to design appropriate studies to meet regulatory requirements, ultimately to meet the project needs. Stay on the top of project with continues scientific and technical support. Proactively identify potential issues and input the constructive suggestions.?With or without supervision, prepare the regulatory submission documents and dossier writing for analytical/bioanalytical, pharmacology, DMPK, or/and safety assessment parts. Search and prepare scientific references for project needs.?Interact with clients, other key functions/business units within WuXi AppTec to facilitate the project development. Directly communicate (visiting host, holding TC and auditing, etc.) with national and international sponsors.?Dynamic study results discussion and consultation: Based on the collected updating data/results, RTPM will continually tune up the studies and process during the progress of project for the best outcome.Qualifications:?Ph.D with 5 years and up or Master with 8 years and up relevant experience in in vitro /in vivo, CMC, or pharmacology, or DMPK, or safety pharmacology, or toxicology, or bioanalytical, experience on biologics will be plus?Project manager experience (manage the preclinical program) must?Biological science education background?Experience in vitro or in vivo studies in research and drug discovery?Regulatory background?Regulatory writing experience will be a plus?Excellent English and Chinese in verbal and writing?Good interpersonal skill and teamwork spirit?Accountability?Capability to research and search information?Potential for personal development within a short timeframe. 职能类别： 生物工程/生物制药
联系方式
上海
公司信息
任仕达集团(Randstad Group) 成立于1960年，是全球最大的综合性人力资源服务机构之一，总部位于荷兰阿姆斯特丹。在全球40多个国家和地区设有4700多个分支机构，每天为57万名求职者提供工作岗位。2011年，其全球营业额达到162亿欧元，位列全球财富500强。 任仕达自2005年进入中国市场，总部设在上海，在华北、华东、华南等地区成立了多个分支机构，服务网络覆盖全国100多个一、二线城市，向企业提供包括搜寻与甄选、灵活派遣以及人力资源解决方案在内的全方位人力资源服务。 作为一家充满活力的专业招聘机构，任仕达始终坚持以人为本，不断追求创新。我们寻找才智过人、诚实可靠、胸怀抱负的求职者，把他们推荐给最适合的企业，帮助他们获得最具吸引力的薪酬和工作机会。 无论您是想拓宽职场发展之路，或是寻找正确的职业发展方向，我们的招聘顾问都会随时为您提供服务。 有了我们的协助，美好职业志在必得。 想了解更多详情，请登录任仕达中国网站www.randstad.cn，或在新浪微博上@任仕达，与我们互动。 www.randstad.cn
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