Clinical Research Associate — Global Trials & Career Growth

IQVIA Argentina; Fatih; Sur place; TRY 180 000 - 230 000; Plein temps

Avantages offerts par ce poste

Company car

Mobile phone

Attractive benefits package

Résumé du poste

IQVIA Turkey is seeking a Clinical Research Associate to join our sponsor-dedicated team as an experienced CRA. The role offers exposure to multiple therapeutic areas and supports career growth within a global organization.

Responsibilities include site visits (selection, initiation, monitoring, close-out), recruitment planning, regulatory compliance, data query resolution, and cross-functional collaboration with study sites and client representatives.

Qualifications

• Requires at least 6 months of on-site monitoring experience.
• Experience in Pharma Industry, and/or Clinical Trials environment
• Excellent command of Turkish and English language, Turkey based
• Driver’s license class B

Responsabilités

• Performing site selection, initiation, monitoring and close-out visits
• Supporting the development of a subject recruitment plan
• Evaluating the quality and integrity of site practices in accordance with regulatory requirements
• Managing progress by tracking regulatory submissions, recruitment, case report form completion, and data query resolutions
• Collaborating with experts at study sites and with client representatives

Connaissances

On-site monitoring

Turkish & English language

MS Office

Organizational skills

Time management

Problem-solving

Travel ability

Formation

University degree in scientific discipline or health care

Outils

MS Office

Description du poste

IQVIA Turkey is seeking a Clinical Research Associate to join our sponsor-dedicated team as an experienced CRA. The role offers exposure to multiple therapeutic areas and supports career growth within a global organization.

Responsibilities include site visits (selection, initiation, monitoring, close-out), recruitment planning, regulatory compliance, data query resolution, and cross-functional collaboration with study sites and client representatives.