加入科默
Join CAREMO
欢迎每位有责任心、有创造力、有执行力的小伙伴加入Caremo family！
CRA
Job Responsibilities:
1. Responsible for clinical trial monitoring, ensuring that all trials are strictly conducted in accordance with the clinical trial protocol, standard operating procedures/internal operating procedures, and applicable regulations.
2. Perform comprehensive monitoring and liaison management for assigned study sites, completing the initiation, execution, and closure of clinical trials at these sites on time.
3. Develop monitoring plans and prepare monitoring reports to ensure clinical research progresses according to schedule.
4. Assist senior supervisors in selecting trial sites for assigned projects and controlling trial budgets.
5. Serve as an external representative of the company and clients, effectively communicating important company and client information to investigators (physicians), and fostering and maintaining good relationships with them.
Job Requirements:
1. Bachelor's degree or above in medicine, pharmacy, or related fields.
2. More than two years of experience in a similar role.
3. Responsible, diligent, grounded, and proactive.
4. Strong learning ability and execution capability.
Based in:
Nanjing, Lianyungang, Zhengzhou, Lishui, Wuhan, Tianjin, Jinan
Follow us
Contract Us：
Add：Building C6, No. 9, Weidi Road, Qixia District, Nanjing
P.C：210046
Tel：025-85760569
M.P：bd@caremo.com.cn
