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
• 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

Benefits

• Health and welfare benefits