Clinical Research Associate II (CRA II) - Hybrid

About the role

ICON Strategic Solutions is hiring a CRA II in a sponsor-dedicated model, supported by ICON's global expertise. As the world's largest FSP organisation, with over 90 sponsor partnerships, ICON offers stability, career development and a collaborative environment where your work contributes to treatments that benefit patients worldwide. The role involves designing and analysing clinical trials and interpreting complex medical data.

Key responsibilities

• Contribute to clinical trial monitoring activities, taking responsibility for your deliverables and working collaboratively.
• Carry out site qualification, initiation, monitoring and close-out visits for clinical trials.
• Ensure protocol compliance, data integrity and patient safety throughout the trial.
• Work with investigators and site staff to ensure smooth study conduct.
• Review data and resolve queries to maintain high-quality clinical data.
• Help prepare and review study documentation, including protocols and clinical study reports.

Required profile

• Bachelor's degree in a scientific or healthcare-related field.
• Minimum of 2 years of experience as a Clinical Research Associate.
• Willingness to travel approximately 60% of the time.
• Legal right to work in the country where the role is based.

Required skills

• In-depth knowledge of clinical trial processes, regulations and ICH-GCP guidelines.
• Strong organisational and communication skills with attention to detail.
• Ability to work independently and collaboratively in a fast-paced environment.

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.