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Clinical Trial Coordinator

Warsaw, Poland💼 Full-time🗓 2026-07-08 → 2026-09-30

Core

Provide administrative and technical support to clinical trial project teams, ensuring audit readiness and managing study documentation.

Role type

Clinical Trial Coordinator

Builds

End-to-end support for clinical trials from study start-up to close-out

Domain

Clinical Research / Life Sciences

Deliverable

Dashboards & analysis

Required skills

Study documentation management, Regulatory compliance (ICH GCP, Country Regulations), Data analysis and reconciliation, Vendor coordination, Translation support, System administration (eTMF, GoBalto)

Preferred skills

Life Science degree, Experience with clinical trial databases, Proficiency in MS Office

Technologies

eTMF, GoBalto, MS Office (Word, Excel, PowerPoint)

Responsibilities

Perform department and Investigator file reviews, Track local regulatory documents, Transmit documents to client and IRB/IEC, Analyze and reconcile study metrics, Maintain vendor trackers, Assist with Investigator Site File (ISF) compilation

Seniority

Individual Contributor

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