Senior Clinical Research Associate
$110,520–$138,150 year
On-siteTexas, United States or Illinois, United States
Job Summary
Set up and monitor Phase II–IV dermatology and rare disease trials, ensuring adherence to ICH-GCP guidelines. Submit protocol and consent documents for ethics/IRB approval, prepare regulatory submissions, and balance sponsor-generated queries. Maintain documentation, complete reports, and prepare feasibility studies for new proposals while driving study cost efficiency. Assist in training and mentoring fellow CRAs. Requires 18+ months of monitoring experience in Phase I–III trials, a degree in medicine or science, and fluency in German and English. Travel 60% of the time (international and domestic).
Required Qualifications
- 18 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
- Excellent written and verbal communication in German & English
- Ability to work to tight deadlines
- Availability to travel least 60% of the time (international and domestic -fly and drive)
- Valid driving license
- Employment with ICON is contingent upon having the legal right to work in the country where the role is based
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