Cra I, Cra Ii, Or Senior Cra (Single-Sponsor)

CRA I, CRA II, or Senior CRA (Single-Sponsor) ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.
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.
The role: Independent, proactive work to set up and monitor studies, complete reports and maintain documentationSubmitting protocol, consent documents for ethics/IRB approval, as well as preparing regulatory submissionsBalancing sponsor generated queriesTaking responsibility for study cost efficiencyPreparation and review of study documentation and feasibility studies for new proposalsPotential to assist in training and mentoring fellow CRAsYou will need: 10 months+ of monitoring experience in phase I-III trials as a CRACollege degree in medicine, science, or equivalentPrevious monitoring experience in medium-sized studies, including study start-up and close-outKnowledge of ICH-GCP guidelines and ability to review and evaluate medical dataExcellent written and verbal communicationAbility to work to tight deadlinesAvailability to travel at least 60% of the time (international and domestic -fly and drive) and should possess a valid driving licenseICON is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

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