We are seeking a Clinical Research Site Coordinator based in Ankara to support upcoming projects. You will work closely with principal investigators, ensuring all drug trials adhere to ICH-GCP guidelines and local regulations.
Key Responsibilities
- Monitor and oversee study sites to guarantee compliance with ICH-GCP and relevant legislation
- Organize and coordinate clinical center activities for each protocol
- Serve as the main liaison between the study team and site personnel
- Ensure accurate and timely medical documentation and reporting
Qualifications
- At least 2 years of hands-on experience in clinical research site management
- Bachelor’s degree in a health or life sciences field (e.g., Biology, Chemistry, Biochemistry, Molecular Biology and Genetics)
- Proficiency in MS Office applications
- Strong command of English (reading, writing, and speaking)
- Detail-oriented approach to documentation and reporting processes
- Excellent interpersonal and presentation skills
- Available for full-time work in Ankara