Are you a Clinical Research Associate or Senior Clinical Research Associate looking for a new and exciting challenge with exposure to ongoing support and growth? Then we have the job for you!IQVIA’s Clinical FSP/Client Focused Department has new upcoming (S)CRA positions with our ongoing and newest clients across Australia and New Zealand.As a CRA within this model you will be responsible for the following(but not limited to)::Contribute to the identification of new sites for clinical trials; analyse capability and support CRMA and CSM in making recommendation for trial inclusion.Assume ambassadorial role to facilitate communication between sites and the client CPO to increase value proposition to investigators.Facilitate the preparation and collection of site and country level documents during all phases of the trial. Supports the CSM in the oversight of Country and Site Trial Master Files (TMF). During all phases of the trial ensure archiving per relevant SOP.Negotiate investigator remuneration; prepare financial contracts between the client and investigational sites and investigators.Ensure adherence to payment schedule.Execute site initiation and training, generate initiation visit report.Implement complete site management including monitoring visits, regulatory assessment, drug supply management, etc. to ensure compliance with protocol, GCP, global and local regulations, global and local processes.Identify problems at sites; resolve issues and escalate as appropriate.Collaborate with the CSM to ensure recruitment and execute contingency plans, as needed.Complete preparation and generation of visit monitoring reports as per relevant SOPReview and manage data at site; resolve technical and content issues on a continuous basis in order to achieve timely database lock targets.If working with central CRAs (blinded and un-blinded), respond to alerts and follow-up to ensure resolution of issuesImplement site close-out activities and generate site close-out report.Provide feedback on site performance for future trial site feasibility/selectionRequired skills and experience:Bachelors Degree in Life Sciences or other scientific/nursing disciplines is essentialMinimum of 2 years Clinical Research Associate experience, preferable within a CRO or PharmaAbility to travel on a regular basis which will involve interstate travel across ANZExtensive knowledge of Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines is requiredOncology experience is highly desiredShould this position be of interest or should you know anyone who may be interested please submit a resume and cover letterPlease note these positions are only available to candidates who have current Australian Working Rights and live within the desired locationIf you are suitable for this position a member of the Talent Acquisition team will be in contact to discuss your applicationIf you wish to hear more about these positions or any other positions IQVIA is currently advertising please reach outSydney +612 9016 8100Melbourne +613 9519 6800Auckland NZ +64 9440 6200At IQVIA, 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. The advanced analytics, technology solutions and contract research services we provide to the life sciences industry are made possible by our 67,000+ employees around the world who apply their insight, curiosity and intellectual courage every step of the way.