Clinical Research Associate
7 days 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, and we welcome you to join us on our mission to shape the future of clinical development.
Role Requirements:
- 12+ months of independent monitoring experience as a CRA.
- Fluent in French and English.
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./>• Submitting protocol, consent documents for ethics/IRB approval, as well as preparing regulatory submissions.
• Potential to assist in training and mentoring fellow CRAs.
You will need:
• 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.
• Availability to travel at least 60% of the time (international and domestic - fly and drive) and should possess a valid driving license.
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