(Senior) Clinical Research Associate - Sponsor-Dedicated
Location: Turkey (Nationwide) - Istanbul or Izmir are preferred locations
Employment Type: Full-time, Permanent
Join a leading global CRO, currently partnering with a major sponsor on long-term clinical trials across multiple therapeutic areas. This is a position offering the structure, training, and support of a global organization, while providing the opportunity to work closely with one client and gain deep exposure to their studies and systems.
Key Responsibilities:
- Conduct site selection, initiation, monitoring, and close-out visits
- Ensure compliance with GCP, ICH guidelines, and local regulations
- Support patient recruitment and site performance strategies
- Track regulatory submissions, case report forms (CRFs), and data query resolution
- Collaborate closely with investigators, study site staff, and sponsor stakeholders
Requirements:
- Degree in a life sciences or healthcare-related field
- Previous working history within independent on-site monitoring
- Strong knowledge of clinical research regulations and GCP
- Fluent in Turkish and English (written and verbal)
- Proficient in MS Office
- Excellent organizational and time management skills
- Ability to build strong site and internal relationships
- Flexibility to travel as required
- Valid driver's license (Class B)
What's on Offer:
- Dedicated training and mentoring programs to support career development
- Access to global resources and operational support
- Exposure to a wide range of therapeutic areas and study phases
- Flexible work-life balance
- Competitive salary, company car, phone, and comprehensive benefits package
- Stable role with an international CRO and long-term client partnership
If you are having difficulty in applying or if you have any questions, please contact Theodora Savlovschi-Wicks at theodora@proclinical.com.
If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists please request a call back at the top of this page.
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