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 in line with project needs.
• Administer protocol and related study training to assigned sites and establish regular lines of communication with sites.
• Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations.
• Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution.
• Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans.
• Collaborate and liaise with study team members for project execution support.

Benefits

• Competitive base pay range ($87,200.00 - $145,300.00)
• Incentive plans, bonuses, and/or other forms of compensation
• Range of health and welfare and/or other benefits