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IQVIA is a global provider of clinical research services, commercial insights, and healthcare intelligence for the life sciences and healthcare industries. The company is seeking a CRA 2, Oncology, to conduct on-site clinical trial monitoring, manage study progress and documentation, support subject recruitment, and ensure compliance with protocols and regulatory requirements. Responsibilities Perform site monitoring

Responsibilities Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements Perform site monitoring visits (selection, initiation, monitoring, and close-out visits) in accordance with contracted scope of work and Good Clinical Practice Work with sites to adapt

Responsibilities Conduct all phases of site monitoring activities, including site selection, initiation, routine monitoring, and close-out visits Evaluate site performance and ensure adherence to study protocols, GCP, ICH guidelines, and applicable regulatory requirements Partner with investigative sites to develop, implement, and track patient recruitment and retention strategies that support enrollment goals Delive