CRA 2, Oncology, IQVIA

Requirements

• Perform site monitoring visits in accordance with contracted scope of work and regulatory requirements
• Work with sites to adapt, drive, and track subject recruitment plan
• Administer protocol and related study training to assigned sites
• Evaluate the quality and integrity of study site practices
• Manage the progress of assigned studies by tracking regulatory submissions and approvals
• Ensure copies/originals site documents are available for filing in the Trial Master File (TMF)
• Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans

Benefits

• Paid time off
• 401(k) matching
• Health and welfare benefits
• Incentive plans, bonuses, and/or other forms of compensation