Regional Monitor (Clinical Research Associate)

ment review and discrepancy resolution and prevention support * Preparing and editing visit reports within the allotted timeframe * Other duties, as required.QUALIFICATIONS & REQUIREMENTS: * 5+ years of experience as a Regional Monitor CRA, including a minimum of two years of cardiovascular device trials (cardiology-specific devices preferred) * Familiarity with ICH, GCP and FDA guidelines and requirements * Good written, verbal and interpersonal communication skills & solid computer skills, including MS Office, EDC, eTMF and Excel trackers (must be able to ramp up quickly on custom trackers) * Relevant bachelor's degree. * Clinical Research Certification and experience with and understanding of cath reports and cath logs and are big plusesLOCATION: Work will be performed remotely from home and at study sites in the Western United States