PM clinical project manager


1. Bachelor degree or above in clinical medicine, pharmacy or related field

2. Be familiar with ich-gcp and new drug research and development processes, proficient in drug and instrument management related regulations, clinical research and clinical research supervision procedures. Have a thorough understanding of the clinical study of drugs and devices, and be familiar with the safety regulations related to clinical research. Received systematic clinical study procedures and regulatory training, familiar with international well-known pharmaceutical companies or CRO and clinical research related SOP/WI

3. More than 4 years of clinical research experience, familiar with clinical research from the beginning to the end of the study, familiar with all types of clinical supervision, ethical submission and contract negotiation. To manage at least one or more domestic registered clinical studies or phase I projects independently

4. Experience of I/BE is preferred

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