Clinical Research Associate II

September 27

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Description

• Monitor and own the progress of clinical studies • Ensure clinical studies are conducted per protocol, SOPs, and regulations • Coordinate activities required to set up and monitor a study • Work with 2-3 protocols on average and support Project Managers

Requirements

• 4-year college degree or equivalent experience • 2+ years CRA experience within the CRO or pharmaceutical industry • Experience in monitoring Lupus and/or Cardiology • Availability for domestic travel including overnight stays, up to 50-60% travel commitment • Fluency in English

Benefits

• Paid time off • Volunteer time off • Robust medical offerings • Non-vested 401k plus company match • Paid parental leave • Numerous other benefits

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