Delivering clinical trial monitoring work to a high standard
Working closely with team and stakeholders
Coordinating 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 English
Good social skills enabling you to deal with queries in a timely manner
Willingness to travel as required (approximately 60%)

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

Clinical Research Associate

Key skills