Research Coordinator
2 weeks ago
At ICON, we're proud to foster an inclusive environment driving innovation and excellence. As a Senior CRA in Canada, you'll play a key role in shaping the future of clinical development.
About the Role:
- You will be responsible for 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 is also a part of this role.
- Balancing sponsor-generated queries and taking responsibility for study cost efficiency are essential tasks.
- You will also prepare and review study documentation and feasibility studies for new proposals.
- Potential opportunities to assist in training and mentoring fellow CRAs exist.
Your Background:
- You should have 12+ months of monitoring experience in phase I-III trials as a CRA.
- A college degree in medicine, science, or equivalent is required.
- Previous monitoring experience in medium-sized studies, including study start-up and close-out, is necessary.
- You should have knowledge of ICH-GCP guidelines and ability to review and evaluate medical data.
- Excellent written and verbal communication skills are required.
- Ability to work to tight deadlines and travel at least 60% of the time (international and domestic) is essential.
What We Offer:
We offer a competitive salary of $80,000 - $100,000 per year, depending on experience.
About ICON:
ICON plc is a world-leading healthcare intelligence and clinical research organization. Our diverse teams enable us to become a better partner to our customers and help us to fulfill our mission to advance and improve patients' lives.
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