深圳招聘

职位描述：
Responsbility:
1.Oversight and project management of assigned clinical trial protocol(s) to ensure patient safety, quality and timely study execution in accordance with prevailing laws, Good Clinical Practices, and Jecho standards.
2.Responsibility include: project assessment and initiation, resource procurement and planning, project implementation, leading and motivating a cross-functional team, milestone planning and tracking, ensuring production of key project progress reports, oversight of communications between Jecho and CRO, and contract and financial management.
？- Protocol feasibility and site selection
？- Full service CRO oversight
？- Quality review site visits/co-monitoring
？- Study and site management interface
？- Regulatory / ethics / health authority responsibilities
？- Inspection readiness, compliance and audit responsiveness
Requirements:
- A scientific or technical degree in the healthcare area is preferred along with extensive knowledge of clinical trial methodology:BSc/MSc/ Ph.D./MD or equivalent;
- Solid knowledge of clinical development processes;
- Site Management/Monitoring (CRA) experience，CRO management experience is preferred;
- Project management experience in the clinical development area;
- 3-6 years of clinical research experience;
- Demonstrated knowledge of clinical research processes and regulatory requirements; ability to gain command of process details
- Knowledge and demonstrated success in training and implementation
- Demonstrated ability to manage complex projects and cross-functional processes required
- Highly proficient verbal and written communication skills (Chinese and English) 举报 分享

  杰科生物成立于2015年，公司坐落于天津滨海新区中新生态城。

  杰科生物产业定位于高端生物医药，产品涵盖单克隆抗体、重组蛋白、溶瘤病毒、免疫毒素、疫苗等。依托于我们可持续的强大创新研发实力、备受业界推崇的设备设施配置、遵循GMP的全过程管理体系以及最重要的——不断壮大的优秀人才团队，我们从研发、生产到上市，覆盖生物医药产业全链条。

  杰科生物致力于研发生产创新医药，在满足自身发展的同时，我们积极面向全球客户展开共赢合作，为客户定制和提供优质产品和增值服务，乃至完整的解决方案。