Senior Clinical Research Associate (Freelance, up to 0.5 FTE)

About the role

We are seeking an experienced, unblinded Senior Clinical Research Associate on a freelance basis (up to 0.5 FTE) to support additional study requirements in Turkey. The role involves comprehensive clinical monitoring, site management, and regulatory oversight for assigned protocols.

Key responsibilities

• Conduct all types of monitoring visits (initiation, interim, close‑out) both in‑person and remotely, and produce monitoring reports in line with SOPs and local regulations.
• Perform study start‑up activities such as site feasibility, ethics committee submissions, and preparation of essential site documents.
• Review source documents and case report forms for accuracy, resolve data issues, and manage investigational supplies.
• Communicate with investigators, site staff, and internal teams to address monitoring and regulatory needs, and participate in project meetings.

Required profile

• Minimum Bachelor’s degree or equivalent experience.
• More than 5 years of experience as a Clinical Research Associate.
• Strong organizational skills, attention to detail, and ability to work with minimal supervision.

Required skills

• Proficiency with Microsoft Office (Outlook, Word, Excel, PowerPoint).
• Hands‑on experience with Electronic Data Capture (EDC), Clinical Trial Management System (CTMS), IVRS, and eTMF platforms.
• Knowledge of local Turkish regulations, ICH guidelines, and GCP standards.