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IQVIA
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(Senior) Clinical Research Associate - Sponsor dedicated - Türkiye
Turkey
· Full-time
·
Not Applicable
Senior Clinical Research Associate
IQVIA is the Human Data Science Company oriented to drive human health outcomes forward.
When you join IQVIA Turkey as a sponsor-dedicated CRA, you’ll enjoy the stability and resources of a leading, global contract research organization while gaining direct experience with one of our customers.
With access to world-class training and mentoring, you’ll have the opportunity to put your passions to work in an environment designed to help you gain experience in a wide variety of therapeutic areas.
Your Responsibilities Will Include
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
IQVIA is the Human Data Science Company oriented to drive human health outcomes forward.
When you join IQVIA Turkey as a sponsor-dedicated CRA, you’ll enjoy the stability and resources of a leading, global contract research organization while gaining direct experience with one of our customers.
With access to world-class training and mentoring, you’ll have the opportunity to put your passions to work in an environment designed to help you gain experience in a wide variety of therapeutic areas.
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
- 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
- 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 stabile, international, reputable company
- Company car, mobile phone and attractive benefits package
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
Key Skills
Ranked by relevance
gcp
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- Posted
- Apr 13, 2026
- Type
- Full-time
- Level
- Not Applicable
- Location
- Istanbul
- Company
- IQVIA
Industries
Hospitals
Health Care
Categories
Research
Analyst
Information Technology
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3 roles aligned with this opportunity
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Machine Learning Engineer II
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Junior HR Operations & Reporting Analyst (m/f/d)
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