Experienced Clinical Research Associate – Istanbul, On-Site

IQVIA; Fatih; On-site; TRY 360,000 - 500,000; Full time

Benefits offered by this job

Company car

Mobile phone

Benefits package

Job summary

IQVIA Turkey is seeking an Experienced Clinical Research Associate to join our Sponsor dedicated team in Istanbul. You will perform site selection, initiation, monitoring and close-out visits, while supporting subject recruitment plans and ensuring regulatory compliance under GCP/ICH guidelines.

You will track submissions, recruitment progress, CRF completion and data queries, collaborating with site staff and client representatives across therapeutic areas.

Qualifications

• University degree in scientific discipline or health care.
• At least 6 months of on-site monitoring experience.
• Turkish and English language proficiency; based in Turkey.

Responsibilities

• Perform site selection, initiation, monitoring and close-out visits.
• Support the development of a subject recruitment plan.
• Evaluate site practices for regulatory compliance (GCP/ICH).
• Manage regulatory submissions, recruitment, CRF completion and data query resolutions.
• Collaborate with study sites and client representatives.

Skills

On-site monitoring

Regulatory compliance

GCP/ICH knowledge

Turkish language

English language

Travel readiness

MS Office

Team collaboration

Communication skills

Driver’s license

Education

University degree in science

Tools

MS Office

Job description

IQVIA Turkey is seeking an Experienced Clinical Research Associate to join our Sponsor dedicated team in Istanbul. You will perform site selection, initiation, monitoring and close-out visits, while supporting subject recruitment plans and ensuring regulatory compliance under GCP/ICH guidelines.

You will track submissions, recruitment progress, CRF completion and data queries, collaborating with site staff and client representatives across therapeutic areas.