Clinical Research Associate II - FSP

📋 Description

• Oversees all aspects of study site management to ensure patient safety is protected, quality of
• Provides guidance at the site and project level towards audit readiness standards and supports
• Updates, tracks and maintains study specific trial management tools/systems, and status reports.
• If required, manages site start up procedures including the feasibility and recruitment of
• If required, assists the negotiation of study budgets and the execution of investigator contracts
• Verifies the process of obtaining informed consent has been adequately performed and documented for

🎯 Requirements

• 4-year college degree or equivalent experience in a scientific or healthcare discipline.
• Two (2) years or more as a CRA in a CRO or equivalent, relevant experience and/or demonstrated
• Excellent communication and organizational skills are essential. A team player.
• Evidence of a client focused approach.
• Experience using computerized information systems, electronic spreadsheets, word processing and
• Ability to travel overnight. Up to 60% travel on average, based on regional requirements.

🎁 Benefits

• Paid time off
• Volunteer time off
• Robust medical offerings
• Non-vested 401k plus company match
• Paid parental leave
• Discretionary annual bonus