上海招聘

Clinical Research
- Develop appropriate programme profiles and programmes to support research recommendations and meet local registration requirements, and provide disease and programme training to CTA/CRC.
- Develop local ICF (informed consent document) and translate as required.
- Prepare and deliver product and program presentations at the investigator's meeting and answer questions from the investigator.
- Act as clinical director in the research team, review and approve subject eligibility and project deviation, review study medical data, analyze adverse events/serious adverse events and answer clinical and product inquiries from researchers.
- Provide input in the final determination of SAP (statistical analysis plan) and strive for database cleansing

Regulatory support
- Prepare clinical documentation as needed to respond to CDE query.
- Prepare slides as needed and deliver presentations to the CDE review meeting for the clinical section

任职要求：
Bachelor degree or above with major in clinical medicine/related
3 year's working experience in clinical medicine within at least 1 year's experience in clinical trial
2-3 year's experience in clinical protocol（Phase 1-3,prefer oncology project background

    江苏晨泰医药科技有限公司成立与2017年1月，是一家专注于研发创新疗法以满足医疗急需的临床研究阶段的公司。公司的管理团队在肿瘤治疗、临床运营、注册事务、医药营销等医学研究方面有几十年经验。目前在上海、北京设有办事处。
    2018年6月19日，晨泰医药科技有限公司（“晨泰医药”）宣布其成功完成A轮6,500万美元融资的首次交割，共计3,700万美元。这次融资由国内知名风险投资机构启明创投领投。其他几家知名的投资公司也参与了这一轮融资，其中包括泰福资本和醴泽健康产业投资基金。A轮募资将用于开展公司主要在研产品AZD3759的国际多中心II期临床试验，和进一步丰富公司的产品管线。
   为致力于全球化创新药物的临床开发。公司与国际大型制药公司合作, 确保产品的前期研发工作扎实可靠。利用公司强大的科学顾问和管理团队，制定最优化的创新药物开发策略，注重研发/市场/知识产权保护的多维布局。具体试验操作和业务开展方面与国际/国内顶尖的CRO/CMO/医院/研究院所合作，使用公司完善的项目管理体系来协调、监督项目合理有序开展。