Clinical Research Associate (CRA I)

About the role

ICON Strategic Solutions is hiring a Clinical Research Associate (CRA I) in Tel Aviv. You will work in a sponsor-dedicated model, contributing to the clinical trial operations function and helping deliver high-quality outcomes across clinical programmes. The role involves delivering clinical trial monitoring work to a high standard, working closely with your team and stakeholders.

Key responsibilities

• Coordinate all activities for setting up and monitoring a study, complete accurate study status reports and maintain study documentation
• Run sponsor-generated queries efficiently and take responsibility for study cost efficiency
• Participate in preparing and reviewing study documentation and feasibility studies for new proposals as required
• Build strong, collaborative relationships with key stakeholders, clinical investigators and site staff
• Ensure patient safety by complying with ICON's procedures, protocols and regulatory requirements

Required profile

• Relevant clinical trial monitoring experience
• University degree in medicine, science or equivalent
• Willingness to travel approximately 60% of the time
• Legal right to work in the country where the role is based

Required skills

• Knowledge of ICH-GCP guidelines and ability to review and evaluate medical data
• Excellent written and verbal communication in English
• Good social skills for handling queries in a timely manner

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