Clinical Research Associate (CRA II) – Clinical Trials

About the role

ICON is a global healthcare intelligence and clinical research organisation seeking a CRA II to design and analyse clinical trials, interpret complex medical data, and support the development of innovative treatments.

Key responsibilities

• Conduct site qualification, initiation, monitoring, and close‑out visits for clinical trials.
• Ensure protocol compliance, data integrity, and patient safety throughout the trial.
• Collaborate with investigators and site staff to facilitate smooth study conduct.
• Perform data review and resolve queries to maintain high‑quality clinical data.
• Contribute to the preparation and review of study documentation, including protocols and clinical study reports.

Required profile

• Bachelor's degree in a scientific or healthcare‑related field.
• Minimum of 2 years experience as a Clinical Research Associate.
• In‑depth knowledge of clinical trial processes, regulations, and ICH‑GCP guidelines.
• Strong organisational and communication skills with attention to detail.
• Willingness to travel approximately 60% of the time.

Required skills

• Clinical trial monitoring
• ICH‑GCP guidelines

What we offer

• Competitive base salary and performance‑related incentives.
• Health and wellbeing programmes including medical, dental, and vision coverage.
• Retirement and pension plans, life assurance and disability coverage.
• Employee assistance programmes and wellbeing resources.
• Learning and development opportunities through structured training and career pathways.