(Senior) Clinical Research Associate - Sponsor dedicated - Türkiye
On-siteIstanbul, Istanbul, Turkey
Job Summary
Perform site selection, initiation, monitoring, and close-out visits while supporting subject recruitment plan development. Evaluate site practices against Good Clinical Practice and ICH guidelines, then manage progress by tracking regulatory submissions, recruitment, case report form completion, and data query resolution. Collaborate with experts at study sites and client representatives to ensure data integrity. Requires at least two years of on-site monitoring experience, a university degree in a scientific discipline, and excellent Turkish and English language skills. This role offers direct customer experience within IQVIA's global network, providing access to world-class training and mentoring in diverse therapeutic areas.
Required Qualifications
- University degree in scientific discipline or health care
- At least 2 years of on-site monitoring experience
- Good knowledge of clinical research regulatory requirements
- Very good computer skills including MS Office
- Excellent command of Turkish and English language
- Organizational, time management and problem-solving skills
- Ability to establish and maintain effective working relationships with co-workers, managers, and clients
- Flexibility to travel
- Driver's license class B
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