Responsibilities:

• Provide writing support for clinical study protocols、CRF、ICF、laboratory manuals、pharmaceutical manuals and clinical monitoring plan.
• Maintain close contact with clinical centers, submit ICH-GCP and manage contract process.
• Assist PI and clinical centers in patients’ selection, trials launch and communication.

Qualifications:

• Bachelor’s degree or above in Clinical Medicine, Pharmacy or related majors.
• Minimum 1 year’s experience in clinical trial management. Previous experience in oncology project is a plus.
• Experience of clinical research in international multi-centers better.