Senior Clinical Research Associate
$110,520–$138,150 year
On-siteTexas, United States or Montana, United States
Texas, United States or Montana, United StatesOn-siteFull Time$110,520–$138,150 yearSenior LevelAssociates DegreeEnterprise
Full TimeSenior LevelAssociates DegreeEnterprise
Job Summary
Set up and monitor Phase II–IV dermatology and rare disease trials, ensuring adherence to ICH-GCP regulations. Submit protocol and consent documents for ethics/IRB approval while preparing regulatory submissions. Independently manage study start-up, close-out, and cost efficiency, balancing sponsor-generated queries. Prepare and review feasibility studies for new proposals and maintain comprehensive documentation. Submit reports and assist in training and mentoring fellow CRAs. Requires 18+ months of monitoring experience, German/English fluency, and 60% travel availability.
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
- Legal right to work in the country where the role is based
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