1.Independently handle center screening and starting, write reports, and follow up and solve problems encountered during center screening;
2.Independently handle research center closure, write center closure interview reports, and follow up and solve problems encountered during regular interview;
3.Independently prepare and submit Ethics Committee related documents, and write research center level clinical trial documents;
4.Develop budget for research center based on project budget and present it to project manager for approval, and take charge of contract negotiation with research center;
5.Be responsible for TMF management of assigned research center (center level) in accordance with the company’s SOP project requirements, and offer assistance to investigators in ISF management;
6.Independently manage materials, supplies and investigational drug of research center, and be responsible for application, distribution, inventory taking, or scrapping;
7.Keep regular contact with research center in accordance with the company’s SOP projects and requirements, maintain relationships with research center and investigators, and timely find out, report and solve problems of research center;
8.Assist project manager in project management;
9.Assist direct manager in training and management of other CRAs at various levels, and perform management and training of some CRAs as a mentor.

1.Major of clinical medicine, science in nursing, pharmacy or biomedical science, bachelor degree or above;
2.Preference will be given to the one with GCP training certification;
3.With work experience as CRA and familiar with working process and job duties of CRA;
4.Strong sense of responsibility and excellent contingency ability;
5.Strong independent working ability and team-work spirit;