Delivering clinical trial monitoring work to a high standard
Working independently and actively to coordinate all activities for setting up and monitoring a study
Completing accurate study status reports and maintaining study documentation
Running sponsor generated queries efficiently and taking responsibility for study cost efficiency
Participating in the preparation and review of study documentation and feasibility studies for new proposals as required
Developing and maintaining strong, collaborative relationships with key stakeholders, clinical investigators, and site staff
Ensuring patient safety by ensuring compliance with ICON's procedures, protocols, and regulatory requirements

University degree in medicine, science, or equivalent
Knowledge of ICH-GCP guidelines and the expertise to review and evaluate medical data
Excellent written and verbal communication in Hebrew & English
Good social skills enabling you to deal with queries in a timely manner
Willingness to travel as required (approximately 60%)

Various annual leave entitlements
A range of health insurance offerings to suit you and your family’s needs.
Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being.
Life assurance
Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others.

Clinical Research Associate

Key skills