Clinical Research Associate – Future Roles

About the role

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

Key responsibilities

• Perform site qualification, initiation, interim monitoring, and close‑out visits, both on‑site and remotely.
• Review source documents, verify data entry in case report forms, and resolve queries within agreed timelines.
• Manage investigational product inventory, reconciliation, storage, and dispensing according to protocol.
• Maintain Investigator Site Files, reconcile with Trial Master Files, and ensure archiving compliance.
• Support subject recruitment, retention, and awareness strategies, and document all monitoring activities.

Required profile

• Bachelor’s degree or RN in a related field, or equivalent education and experience.
• Knowledge of Good Clinical Practice (GCP) and ICH guidelines, and ability to apply local regulatory requirements.
• Excellent communication and interpersonal skills with the ability to travel up to 75% of the time.
• Willingness to adapt quickly to changing priorities and manage site‑level activities to meet project timelines.

Required skills

• Good Clinical Practice (GCP) and ICH guideline knowledge.
• Experience with electronic data capture (EDC) systems and case report form (CRF) review.
• Investigational product (IP) handling and inventory management.
• Source document review and query resolution techniques.