Clinical Research Associate – 6 Month Contract

About the role

We are seeking an experienced Clinical Research Associate (CRA) to join a leading global Contract Research Organisation on a six‑month contract. The CRA will ensure high‑quality, audit‑ready clinical trial data across multiple investigational sites while adhering to ICH‑GCP, FDA and local regulatory standards.

Key responsibilities

• Perform clinical monitoring and site management activities in line with ICH‑GCP, FDA regulations and SOPs.
• Conduct site visits to verify protocol adherence, regulatory compliance and data integrity.
• Manage essential documentation, including source documents, monitoring reports and regulatory filings.
• Maintain strong relationships with investigational sites, study teams and project managers.
• Support project or clinical team managers on assigned studies and mentor junior staff where needed.

Required profile

• Degree in life sciences, a related scientific field, or a healthcare professional qualification.
• Approximately five years of clinical research monitoring experience.
• Fluent English; additional local language is advantageous.
• Valid driving licence where applicable.

Required skills

• Clinical monitoring
• Site management
• Knowledge of ICH‑GCP guidelines
• Knowledge of FDA regulations