Clinical Research Associate 1
$75,480–$94,350 year
On-siteCalifornia, United States
Job Summary
Coordinate all activities for setting up and monitoring a study, completing accurate study status reports, and maintaining study documentation. Run sponsor-generated queries efficiently while participating in the preparation and review of study documentation and feasibility studies for new proposals. Develop and maintain strong relationships with key stakeholders, clinical investigators, and site staff, ensuring patient safety through compliance with ICON's procedures, protocols, and regulatory requirements. Requires approximately 60% travel. Salary range $75,480.00-$94,350.00.
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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