Research Analyst

• 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 (i.e., identify investigators; helping prepare regulatory submissions, conducting pre-study and initiation visits, etc.)
• Handle appropriately sized clinical trials, and support Project Managers with trials that are larger in scope
• Train and mentor junior staff members
• Interact directly with clients, initiate payments, and participate in proposal activities, including development and client presentations

Clinical Research Associate II – Senior Clinical Research Associate

Senior Clinical Research Associate II