Regional Monitor (Clinical Research Associate)
REGIONAL MONITOR (12-month, Potential for extension)
SUMMARY:
Clinical Research Associate needed for clinical trial regional monitoring and site management responsibilities for cardiology device research.
DUTIES & RESPONSIBILITIES:
ā¢ Site management, study start-up, communications and scheduling and conducting monitoring visits at clinical study sites.
ā¢ Team meetings and communications
ā¢ Study document review and discrepancy resolution and prevention support
ā¢ Preparing and editing visit reports within the allotted timeframe
ā¢ Other duties, as required.
QUALIFICATIONS & REQUIREMENTS:
ā¢ 5+ years of experience as a Regional Monitor CRA, including a minimum of two years of cardiovascular device trials (cardiology-specific devices preferred)
ā¢ Familiarity with ICH, GCP and FDA guidelines and requirements
ā¢ 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)
ā¢ 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
Apply tot his job
Apply To this Job
SUMMARY:
Clinical Research Associate needed for clinical trial regional monitoring and site management responsibilities for cardiology device research.
DUTIES & RESPONSIBILITIES:
ā¢ Site management, study start-up, communications and scheduling and conducting monitoring visits at clinical study sites.
ā¢ Team meetings and communications
ā¢ Study document review and discrepancy resolution and prevention support
ā¢ Preparing and editing visit reports within the allotted timeframe
ā¢ Other duties, as required.
QUALIFICATIONS & REQUIREMENTS:
ā¢ 5+ years of experience as a Regional Monitor CRA, including a minimum of two years of cardiovascular device trials (cardiology-specific devices preferred)
ā¢ Familiarity with ICH, GCP and FDA guidelines and requirements
ā¢ 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)
ā¢ 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
Apply tot his job
Apply To this Job