Clinical Trial Assistant
Hybrid · Bulgaria
Core
Support clinical research projects by ensuring smooth processes and accurate documentation within a global team.
Role type
Administrative Clinical Process Coordinator
Builds
Trial Master File (TMF) documentation and study records
Domain
Pharmaceutical and clinical research
Deliverable
dashboards & analysis
Required skills
MS Office, data processing, English (fluent), Bulgarian (fluent), document management, vendor coordination, contract review
Preferred skills
Life sciences background, pharma industry experience
Responsibilities
Track site visits in CTMS, perform TMF file reviews and document uploads, manage vendor setup and invoice reviews, coordinate document translations, review contracts, support team queries, provide general administrative support
Seniority
Early-career, administrative support
