Senior CRA - late phase
ICON · Warsaw, Poland +1 more
Clinical OperationsFull-timeCompany career page
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Role summary
Senior Clinical Research Associate overseeing late-phase clinical trial monitoring activities across multiple sites in Poland. Responsibilities include ensuring protocol adherence, conducting site assessments, managing data quality, and mentoring junior staff while working independently from a home base.
What they're looking for
- Bachelor's degree in relevant scientific or healthcare discipline
- Extensive CRA experience with strong clinical trial and regulatory knowledge
- Proven ability to manage multiple sites and projects simultaneously
- Expertise in monitoring practices, data integrity, and clinical trial software
- Strong communication and stakeholder management skills
- Willingness to travel approximately 60% as required
What you'll be doing
- Monitor clinical trial sites for protocol adherence, regulatory compliance, and GCP standards
- Conduct site visits to assess performance, troubleshoot issues, and provide operational support
- Collaborate with cross-functional teams on timely and accurate data collection and reporting
- Train and guide site staff and other CRAs on clinical trial conduct standards
- Build and maintain effective relationships with site personnel to support trial success
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.