Clinical Data Coordinator I
ICON · Warsaw, Poland
BiometricsFull-timeCompany career page
The apply link worked recently (not employer-confirmed).
Role summary
Clinical Data Coordinator I role supporting clinical trial design and data analysis at a global healthcare research organization. The position involves managing clinical data deliverables, collaborating with study teams, and ensuring data quality and regulatory compliance in a hybrid Warsaw location.
What they're looking for
- Master's degree in Life Sciences, Healthcare, or related field
- Basic clinical data management experience in pharmaceutical or biotechnology
- Proficiency with data management software such as Medidata or Oracle RDC
- Strong attention to detail and ability to work in fast-paced environment
- Fluent English and local language proficiency
- Cross-functional collaboration and communication skills
- Knowledge of ICH-GCP regulatory guidelines preferred
What you'll be doing
- Support Data Management Study Lead with eCRF development and data validation specifications
- Review clinical and third-party data according to edit specifications and review plans
- Generate clear and accurate data queries for investigational sites
- Communicate with peers, clinical data scientists, and functional management as needed
- Perform project activities including documentation management and query dispatch to maintain study timelines
Privacy & handoff
This role links to ICON's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.