CRA 2, Oncology, IQVIA

divh2CRA 2, Oncology, IQVIA/h2pColumbus, United States of America | Full time | Field-based | R1537618/ppIQVIA is seeking a CRA 2 with a minimum of 1.5 years of on-site oncology monitoring experience:/ppEssential Functions/ppPerform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines./ppWork with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability./ppAdminister protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues./ppEvaluate 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./ppManage 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 start-up phase./ppEnsure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigators Site File (ISF) is maintained in accordance with GCP and local regulatory requirements./ppCreate 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./ppCollaborate and liaise with study team members for project execution support as appropriate./ppIf applicable, may be accountable for supporting development of project subject recruitment plan on a per site basis./ppIf applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement./ppEducation: Bachelors Degree (Degree in scientific discipline or health care preferred)/ppExperience: 1.5 to 2 years of relevant CRA experience including on-site monitoring./ppIQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide./ppIQVIA 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./ppIQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism./ppThe 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./p/div