Regional Monitor (Clinical Research Associate)

Redbock - an NES Fircroft company

St Paul, MNFull-timePosted Apr 8, 2026

Behavioral Health Market Context

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Job Description

 document 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 pluses

LOCATION:

Work will be performed remotely from home and at study sites in the Western United States

Qualifications

  • 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 pluses

Benefits

    Responsibilities

    • Clinical Research Associate needed for clinical trial regional monitoring and site management responsibilities for cardiology device research
    • Site management, study start-up, communications and scheduling and conducting monitoring visits at clinical study sites
    • Team meetings and communications
    • Study document review and discrepancy resolution and prevention support
    • Preparing and editing visit reports within the allotted timeframe
    • Other duties, as required


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