CRA II / Senior CRA - Hematology Phase I

About the role

ICON is recruiting an experienced Clinical Research Associate (CRA) for a hematology Phase I study in Tel Aviv. The role sits within ICON's clinical trial operations function, working with a dedicated sponsor and contributing to high-quality outcomes across clinical programmes.

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
• Take part in preparing and reviewing study documentation and feasibility studies for new proposals
• 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
• Knowledge of ICH-GCP guidelines and the ability to review and evaluate medical data
• Experience with hematology/rheumatology Phase I studies
• Excellent written and spoken English and good social skills for handling queries promptly
• 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 through structured training and career pathways