Clinical Research Associate – Future Roles

About the role

Syneos Health is seeking a Clinical Research Associate (CRA) to support site qualification, initiation, monitoring and close‑out activities for real‑world late‑phase studies in Turkey. The role involves ensuring compliance with regulatory and ICH‑GCP standards while supporting investigators and study sites.

Key responsibilities

• Perform site qualification, initiation, interim monitoring, and close‑out visits, either on‑site or remotely.
• Assess site performance, manage queries, and ensure accurate data entry in case report forms.
• Conduct source document review, verify informed consent, and protect patient confidentiality.
• Manage investigational product inventory, reconciliation, storage, and dispensing according to protocol.
• Maintain Investigator Site Files, reconcile with Trial Master Files, and document activities per SOPs.
• Support patient recruitment, retention, and provide training to site staff.

Required profile

• Bachelor’s degree or RN in a related field, or equivalent experience.
• Knowledge of Good Clinical Practice (GCP) and ICH guidelines.
• Excellent communication and interpersonal skills.
• Willingness to travel up to 75% of the time.

Required skills

• ICH/GCP Guidelines
• Good Pharmacoepidemiology Practice (GPP)
• Electronic Data Capture (EDC) systems
• Source Document Review
• Investigational Product management