Clinical Research Associate 1
On-siteRaleigh, North Carolina, United States
Job Summary
Coordinate all activities for setting up and monitoring clinical studies, including completing accurate status reports and maintaining documentation. Run sponsor-generated queries efficiently while participating in the preparation and review of study documentation and feasibility studies for new proposals. Develop strong relationships with key stakeholders, clinical investigators, and site staff to ensure patient safety and compliance with protocols and regulatory requirements. This role requires approximately 60% travel and a university degree in medicine or science. Join ICON's global healthcare intelligence organization dedicated to bringing new medicines to patients faster.
Required Qualifications
- University degree in medicine, science, or equivalent
- Knowledge of ICH-GCP guidelines
- Expertise to review and evaluate medical data
- Excellent written and verbal communication in English
- Good social skills enabling you to deal with queries in a timely manner
- Willingness to travel as required (approximately 60%)
- Legal right to work in the country where the role is based
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