Senior Clinical Research Associate – Sponsor Dedicated

About the role

IQVIA Turkey is seeking a sponsor‑dedicated Clinical Research Associate to join its global CRO team. You will work on a variety of therapeutic areas, supporting site activities and ensuring compliance with regulatory standards while gaining exposure to a major client.

Key responsibilities

• Perform site selection, initiation, monitoring and close‑out visits.
• Support development of subject recruitment plans and evaluate site practices against GCP and ICH guidelines.
• Track regulatory submissions, recruitment progress, CRF completion and data query resolution.
• Collaborate with study site experts and client representatives.

Required profile

• University degree in a scientific discipline or health care.
• At least 2 years of on‑site monitoring experience.
• Excellent command of Turkish and English.
• Organizational, time‑management and problem‑solving abilities.
• Flexibility to travel and a valid Class B driver’s license.

Required skills

• Good knowledge of clinical research regulatory requirements (GCP, ICH).
• Very good computer skills, including MS Office.

What we offer

• Career‑growth resources, mentorship and therapeutic training.
• Flexible work schedules and a better work‑life balance.
• Company car, mobile phone and attractive benefits package.
• Potential discretionary sign‑on bonus of up to 210,000 TRY for early starters.