We are currently seeking a Clinical Research Associate 2 to join our dedicated Sponsor team here at IQVIA. Ideally based in Sydney or Melbourne. Previous independent on site monitoring experience is essential for this role.
Key Responsibilities Perform site selection, initiation, monitoring and close-out visits and work with sites to adapt, drive and track subject recruitment plansProvide monitoring visits and site management for a variety of protocols, sites and therapeutic areasAdminister protocol and related study training to assigned sites and establish regular lines of communicationEvaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulationsManage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrolment, 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 plansCollaborate and liaise with study team members for project execution support as appropriate.Not everyone can be a CRA it's an extraordinary role, do you meet this unique criteria? Bachelor's degree in Life Sciences or other scientific/nursing disciplines is essentialMinimum of 2 years independent site monitoring experience for a CRA 2, and a minimum of 4 years independent site monitoring experience for a Sr CRA 1CRO experience is highly desiredAbility to travel on a regular basis which will involve interstate travelExtensive knowledge of Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines is requiredIQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. Learn more at https://jobs.iqvia.com
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