MedTech CRA II: Onsite Monitoring & Study Execution - Travel
Listed on 2026-10-03
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Healthcare
Clinical Research
RQM+ seeks a Clinical Research Associate II to participate in pre-market to post-market clinical trials. You will oversee site qualification, initiation, interim and close-out visits while ensuring GCP compliance and sponsor specifications. Collaborate with CTM and Lead CRA to execute monitoring activities per protocol.
The role requires a Bachelor's degree in a scientific field, 2+ years on-site monitoring, and travel up to 60-75% with strong communication skills and proficiency in MS Office.
This role, Med Tech CRA II:
Onsite Monitoring & Study Execution - Travel at Rqm-, could be your next career step.
If your experience matches this role, we encourage you to apply.
All applications are reviewed carefully by our team.
This is a Full Time role.
The position is based in Town of Texas, WI, United States.
This opportunity is part of our work in Bio & Pharmacology & Health.
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