Clinical Trial Manager

Jan 11, 2022View PDF

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.