As a Clinical Research Associate at ICON, you’ll work within a large-scale, fast-paced environment alongside a close-knit team of highly qualified CRAs to identify, select, initiate and close-out investigational sites for clinical studies in phases II – IV, ensuring adherence to applicable regulations and principles of ICH-GCP.
Compensation
We offer very competitive salary packages. And to keep them competitive, we regularly benchmark them against our competitors. Our annual bonuses reflect delivery of performance goals – both ours and yours.
Responsibilities
Independent, proactive work to set up and monitor studies, complete reports and maintain documentation
Submitting protocol, consent documents for ethics/IRB approval, as well as preparing regulatory submissions
Balancing sponsor generated queries
Taking responsibility for study cost efficiency
Preparation and review of study documentation and feasibility studies for new proposals
Requirements
College degree in medicine, science, or equivalent
Contribute to clinical trial operations by delivering clinical trial monitoring work to a high standard, working collaboratively to deliver high-quality outcomes across clinical programmes.
Compensation
ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.
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 the preparation and review of study documentation and feasibility studies for new proposals
Develop and maintain strong, collaborative relationships with key stakeholders, clinical investigators, and site staff
Requirements
University degree in medicine, science, or equivalent