MedTech CRA II: Onsite Monitoring & Study Execution - Travel
Rqm-
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. #J-18808-Ljbffr Rqm-
Vacancy posted 2 days ago
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