CRA 2, Oncology, Full Service, IQVIA

CRA 2 On-Site Oncology Monitoring

IQVIA is seeking a CRA 2 with a minimum of 1.5 years of on-site oncology monitoring experience. Essential functions include performing site monitoring visits in accordance with contracted scope of work and regulatory requirements, working with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability, administering protocol and related study training to assigned sites, and establishing regular lines of communication with sites to manage ongoing project expectations and issues. The role also involves evaluating the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations, managing the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form completion and submission, and data query generation and resolution, and ensuring copies/originals of site documents are available for filing in the Trial Master File. The candidate should have a Bachelor's Degree in a scientific discipline or health care preferred and 1.5 to 2 years of relevant experience including on-site monitoring.