Clinical Trial Manager

Jun 02, 2021View PDF

Responsibilities:

  • Be responsible for study protocols, CRF, ICF, lab manual, pharmacy manual, clinical monitoring plan.
  • Keep closely relationship with site and submissions for ICH-GCP, site contract process and governor approval.
  • Contribute to PI and site identification, communications, and initiation.
  • Contribute to site feasibility process.

 

Qualifications:

  • Bachelor degree or above in Clinical Medicine/Pharmacy.
  • 1Y+ clinical project management, oncology project experience preferred.

International project experience is preferred.