Experienced Clinical Research Associate - Sponsor dedicated - Türkiye
On-siteIstanbul, Istanbul, Turkey
Job Summary
Conduct site selection, initiation, monitoring, and close-out visits while supporting subject recruitment plans. Evaluate site practices against Good Clinical Practice and ICH guidelines, tracking regulatory submissions, recruitment metrics, case report form completion, and data query resolutions. Collaborate with study sites and client representatives to manage progress. Requires at least six months of on-site monitoring experience, a university degree in a scientific discipline, and a valid driver's license. Excellent Turkish and English skills are essential. Join IQVIA's Sponsor dedicated team in Istanbul, Türkiye, offering a company car and mobile phone.
Required Qualifications
- University degree in scientific discipline or health care
- At least 6 months of on-site monitoring experience
- Experience in Pharma Industry, and/or Clinical Trials environment
- Very good computer skills including MS Office
- Excellent command of Turkish and English language, Turkey based
- 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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