Description
IQVIA is the Human Data Science Company oriented to drive human health outcomes forward.
As a Senior Clinical Research Associate at IQVIA Turkey, you will enjoy the stability and resources of a leading, global contract research organization while gaining direct experience with one of our customers.
Your responsibilities will include:
- 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, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
- Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution
- Collaborating with experts at study sites and with client representatives
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
What you can expect:
- Resources that promote your career growth
- Leaders that support flexible work schedules
- Programs to help you build your therapeutic knowledge
- Better Work-Life balance, optimal DOS
- Excellent working environment in a stable, international, reputable company
- Company car, mobile phone and attractive benefits package
For candidates able to start before September 2026, a discretionary sign-on bonus of up to 210,000 TRY may be offered, with the final amount confirmed at offer stage, subject to role level and relevant experience.