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Clinical Research Associate 2
1 month ago
As a Clinical Research Associate 2, you will be part of a dynamic team responsible for the initiation, monitoring, and closure of assigned sites in clinical studies. You will work closely with sponsors, investigators, and study coordinators to ensure compliance with international guidelines and local regulations.
- Monitor multiple Phase I, II, III, and IV clinical trial sites across different therapeutic areas.
- Collaborate with the team to develop commitment to study timelines and objectives through regular visits with site staff.
- Review source data to ensure patient safety and data integrity.
- Escalate concerns or issues to other departments as appropriate.
Requirements:
- Bachelor's Degree (or equivalent)
- Minimum 2 years of independent on-site monitoring experience or experience as a field CRA
- Ability to travel nationally with overnight stays
- Experience conducting all types of monitoring visits
- Demonstrated working knowledge of ICH/GCP Guidelines
- Excellent record-keeping skills and attention to detail
What ICON Can Offer:
- Competitive salary
- Range of health insurance offerings
- Competitive retirement planning offerings
- Global Employee Assistance Programme
- Life assurance
At ICON, diversity, inclusion, and belonging are fundamental to our culture and values. We're proud of our diverse workforce and the work we've done to become a more inclusive organization.