Senior CRA – Lead Your Own Sites! Sponsor Facing with Full Site Ownership Early-Phase & Pivotal Trials Large Portfolio Across Multiple Therapeutic Areas In this Senior CRA opportunity, you will step into an exciting new challenge owning your studies, lead clinical activity across phase I -III across multiple Therapeutic Areas, while being valued for your operational insight. Our high-growth clinical research client is based in Auckland, renowned or its early-phase portfolio, strong site relationships, and empowering work culture. The Opportunity: Independently monitor sites across NZ (SIVs, IMVs, COVs) for Phase I–III studies Build strong site relationships with PIs, coordinators, and trial teams Verify ICF, AE/SAE documentation, source data, and IMP accountability Collaborate with project management, regulatory, and data teams to drive trial timelines Identify and address site-level risks, deviations, and GCP compliance gaps Contribute to TMF accuracy, CAPAs, and regulatory submissions Requirements: 4 years’ independent monitoring experience, from site selection to close out Phase II/III trial exposure Excellent communication skills with the ability to train, influence, and manage site staff Salary & Package $100,000 - $130,000 DOE (NZ Dollars) If you're looking for autonomy, professional growth, and meaningful sponsor impact then please share your CV to Eve Cooke at ecooke@hpgconnect.com or call me for a confidential conversation on +61 2 8877 8722.
