- Belgrade, Central Serbia, Serbia
Lead initiation and activation activities for clinical studies in Serbia, managing site relationships, regulatory submissions, and trial master file documentation.
Responsibilities
- Act as direct point of contact with assigned sites during start‑up phase
- Build relationships with investigators and site staff
- Support country‑specific feasibility and pre‑qualification activities
- Prepare, negotiate, and facilitate execution of Confidentiality Agreements
- Conduct remote Qualification Visits
Requirements
- Educated to degree level (biological science, pharmacy, or other health‑related discipline) or equivalent nursing qualification