该职位来源于猎聘
Primary Responsibilities
- Develop product clinical development strategy and executive plan under appropriate departmental supervision.
- Skilled in organizing and writing materials related to medical clinical trials of CDE communication meetings, attending face-to-face meetings and communicating with CDE experts when necessary.
- Establish good communication relationship with medical experts in key fields, and close communication about research programs.
- Draft, review, and QC of clinical documents to ensure compliance of documentation to GCP, SOPs.
- Development medical supervision plan and function as a medical monitor in case of need, to ensure the quality and safety of the project, including but not limited to the monitoring of SAE and programme deviation.
- Work closely with CO, RA, BD, PV and other departments, provide advice, support and assistance according to project needs (select of leading
PI/ Participate in project meetings and protocol discussion).
- Serve as primary technical contact with client under appropriate departmental supervision.
- Provide medical professional guidance to subordinates.
Qualification:
- Ph.D. in Medical Science, More than 1 years clinical experience in oncology or chronic disease therapeutic area.
- Or master degree major in medical science, More than 3 years clinical experience in oncology or chronic disease therapeutic area.
- Or bachelor degree in medicine, More than 5 years clinical experience in oncology or chronic disease therapeutic area.
- Be familiar with the key points of clinical trials and relevant policies and regulations.
- Languages: Excellent written and read English Excellent oral
English are preferred.