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Clinical Research Associate II
3 days ago
Description
• Monitor and own the progress of clinical studies at investigative sites • Ensure that clinical studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP, and all applicable regulations and standards • Coordinate all necessary activities required to set up and monitor a study • Work with 2-3 protocols on average and support Project Managers with trials • Interact directly with clients, initiate payments, and participate in proposal activities
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 approximately 50-60% travel commitment • Fluency in English and local language where applicable
Benefits
• Discretionary annual bonus • Health insurance • Retirement savings benefits • Life insurance • Disability benefits • Parental leave • Paid time off for sick leave and vacation
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