CRA 2, Oncology, IQVIA

Responsibilities Perform site monitoring visits (selection, initiation, monitoring, and close‑out) in accordance with the contracted scope of work and regulatory requirements such as Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. Work with sites to adapt, drive, and track subject recruitment plans in line with project needs to enhance predictability. Administer protocol and related study training to assigned sites and establish regular lines of communication to manage ongoing project expectations and issues. Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate. 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. May support the start‑up phase. Ensure copies/originals of site documents are available for filing in the Trial Master File (TMF) and that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements. Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow‑up letters and other required study documentation. Collaborate and liaise with study team members for project execution support as appropriate. May be accountable for supporting the development of a site‑based subject recruitment plan. May be accountable for site financial management according to the executed clinical trial agreement and retrieve invoices according to local requirement. Qualifications Education: Bachelor’s Degree (preferred in a scientific discipline or health care). Experience: 1.5 to 2 years of relevant CRA experience, including on‑site monitoring. Compensation The potential base pay range for this role, when annualized, is $87,200.00 – $145,300.00. The actual base pay offered may vary based on a number of factors including job‑related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part‑time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits. Equal Opportunity Employer IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. #J-18808-Ljbffr IQVIA LLC