Research Coordinator
4 weeks ago
ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence.
We're looking for a highly skilled Senior Clinical Research Associate (CRA) to join our team in Burlington, Canada.
About the Role- Independent, proactive work to set up and monitor studies, complete reports, and maintain documentation
- Submit protocol, consent documents for ethics/IRB approval, and prepare regulatory submissions
- Balancing sponsor-generated queries
- Taking responsibility for study cost efficiency
- Preparation and review of study documentation and feasibility studies for new proposals
- Potential to assist in training and mentoring fellow CRAs
- 12 months+ of monitoring experience in phase I-III trials as a CRA
- College degree in medicine, science, or equivalent
- Previous monitoring experience in medium-sized studies, including study start-up and close-out
- Knowledge of ICH-GCP guidelines and ability to review and evaluate medical data
- Excellent written and verbal communication
- Ability to work to tight deadlines
- Availability to travel at least 60% of the time (international and domestic) with a valid driving license
$70,000 - $90,000 per year, depending on experience.
Benefits of Working with ICONOur success depends on the quality of our people. That's why we've made it a priority to build a culture that rewards high performance and nurtures talent.
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