Site Activation & Start-Up Coordinator

3037 Syneos Health Klinik Arastirma Limited Sirketi; Fatih; On-site; TRY 90,000 - 150,000; Full time

Job summary

Syneos Health is seeking candidates for Site Activation roles in Turkey. You will oversee end-to-end country/site activation, coordinate regulatory submissions, and ensure timely deliverables within the start-up process.

Collaboration with cross-functional teams will be essential to maintain quality and compliance across country submissions and document management. Ideal candidates have a clinical trial background, strong organizational skills, and the ability to manage vendors and complex

Qualifications

• Bachelor’s Degree and understanding of clinical trial processes across Phases II–IV and ICH GCP.
• Ability to manage external vendors and contracts effectively.
• Strong organizational skills and multitasking ability.
• Excellent written and verbal communication in English.
• Ability to work independently as well as part of a team.

Responsibilities

• Ensure quality deliverables at country level; follow project requirements and local rules with oversight.
• Monitor basic financials and hours per contract; escalate discrepancies.
• Comply with SOPs/WIs; keep training records and timesheet compliance.
• Support continuous quality improvement of Site Start-Up components at country level.
• Prepare and submit Central/Local EC, RA applications and other local regulatory submissions.
• Serve as liaison for sites and project leads during start-up on allocated projects.

Skills

Strong organizational skills

Negotiation skills

Independent working

Written & verbal communication

Attention to detail

Education

Bachelor’s Degree, Clinical trial knowledge

Job description

Syneos Health is seeking candidates for Site Activation roles in Turkey. You will oversee end-to-end country/site activation, coordinate regulatory submissions, and ensure timely deliverables within the start-up process.

Collaboration with cross-functional teams will be essential to maintain quality and compliance across country submissions and document management. Ideal candidates have a clinical trial background, strong organizational skills, and the ability to manage vendors and complex