Clinical Research Associate II

About the role

ICON is a global healthcare intelligence and clinical research organisation seeking a Clinical Research Associate 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 process.
• 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 1 year of experience as a Clinical Research Associate on site.
• In‑depth knowledge of clinical trial processes, regulations, and ICH‑GCP guidelines.
• Strong organizational and communication skills with attention to detail.
• Ability to work independently and collaboratively in a fast‑paced environment.
• Willingness to travel approximately 60% of the time.

What we offer

• Competitive base salary and performance‑related incentives.
• Health and wellbeing programmes including medical, dental, and vision coverage where applicable.
• 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.