Senior Clinical Research Associate
ICON · Istanbul, Turkey +1 more
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Role summary
This role involves overseeing clinical trial monitoring activities across multiple sites in Turkey, ensuring compliance with protocols, regulatory standards, and GCP requirements. The Senior CRA will conduct site visits, coordinate data collection, mentor team members, and manage stakeholder relationships. Candidates need a bachelor's degree in a scientific field, extensive CRA experience, strong organizational skills, and willingness to travel approximately 60%.
What they're looking for
- Bachelor's degree in scientific or healthcare-related discipline
- Extensive clinical research associate experience with deep protocol and regulatory knowledge
- Ability to manage multiple sites and projects with strong organizational skills
- Expertise in monitoring practices, data integrity, and site management software
- Excellent communication and stakeholder management abilities
- Willingness to travel approximately 60% as required
What you'll be doing
- Monitor clinical trial sites for adherence to protocols, regulations, and GCP standards
- Conduct site visits to assess performance, resolve issues, and provide operational support
- Collaborate with cross-functional teams on timely and accurate data collection
- Train site staff and other CRAs on clinical trial conduct standards
- Build and maintain relationships with site personnel to ensure smooth trial operations
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.