Remote CRA II: Clinical Monitoring & Site Management

3037 Syneos Health Klinik Arastirma Limited Sirketi; Fatih; Hybrid; TRY 260,000 - 380,000; Full time

Job summary

Syneos Health Türkiye is seeking a CRA II to monitor clinical studies, ensure data integrity, verify regulatory compliance across sites, and support Quality by design, using remote and on-site approaches as needed, with a flexible travel schedule.

You will partner with site teams, sponsors and cross‑functional colleagues, apply risk-based monitoring, implement quality tools, review CRFs and ISFs, and help drive study milestones through proactive communication and timely issue resolution.

Qualifications

• Bachelor’s degree or RN in a related field or equivalent combination of education, training and experience
• Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements
• Must demonstrate good computer skills and be able to embrace new technologies
• Excellent communication, presentation and interpersonal skills
• Ability to manage required travel of up to 75% on a regular basis

Responsibilities

• Oversee and ensure integrity of clinical studies through remote monitoring.
• Conduct remote monitoring to verify regulatory compliance and protocols.
• Collaborate with site teams to implement quality monitoring tools and processes.
• Manage project communication and timelines with sponsors and sites.
• Prepare for Investigator Meetings and maintain audit readiness.

Skills

Communication skills

Presentation skills

Interpersonal skills

Computer skills

Travel willingness

Education

Bachelor’s degree or RN in a related field or equivalent combination of education, training and experience

Job description

Syneos Health Türkiye is seeking a CRA II to monitor clinical studies, ensure data integrity, verify regulatory compliance across sites, and support Quality by design, using remote and on-site approaches as needed, with a flexible travel schedule.

You will partner with site teams, sponsors and cross‑functional colleagues, apply risk-based monitoring, implement quality tools, review CRFs and ISFs, and help drive study milestones through proactive communication and timely issue resolution.