Clinical Research Associate I (CRA I)

About the role

ICON is seeking a Clinical Research Associate I to support clinical trial operations, ensuring high‑quality outcomes across its programmes. You will work within a sponsor‑dedicated model, collaborating with global expertise.

Key responsibilities

• Coordinate study set‑up and monitoring activities, produce accurate status reports and maintain documentation.
• Run sponsor‑generated queries, contribute to cost‑efficiency, and assist with feasibility studies for new proposals.
• Develop strong relationships with investigators, site staff and other stakeholders.
• Ensure patient safety by adhering to ICON procedures, protocols and regulatory requirements.

Required profile

• University degree in medicine, science or equivalent.
• Knowledge of ICH‑GCP guidelines and ability to review medical data.
• Excellent written and verbal English communication.
• Willingness to travel up to 60% of the time.

Required skills

• Clinical trial monitoring.
• ICH‑GCP compliance.

What we offer

• Competitive base salary and performance incentives.
• Health, dental and vision coverage where applicable.
• Retirement and pension plans, life assurance and disability coverage.
• Learning and development opportunities through structured training.