An exciting opportunity is available for an experienced Clinical Trials professional to join a high-performing research team supporting the start-up and activation of clinical studies. This role sits within a dedicated Study Start-Up function and plays a critical part in ensuring trials are launched efficiently, compliantly, and on time. The Opportunity You will take ownership of the end-to-end start-up process, working closely with sponsors, CROs, and internal stakeholders to bring clinical trials from concept to site readiness. Key Responsibilities Act as the primary liaison for Sponsors and CROs during study start-up Manage ethics submissions, governance documentation, and CTNs Prepare and negotiate budgets and Clinical Trial Research Agreements (CTRA) Ensure all regulatory and operational requirements are met prior to site initiation Coordinate vendors, systems, and essential documentation Support smooth handover to operations and participate in cross-functional meetings Contribute to process improvements and maintain accurate tracking systems About You 2 years’ experience in clinical trial start-up or governance Strong knowledge of HREC, SSA, CTN, and CTRA processes Experience working with Sponsors and reviewing trial documentation Highly organised with strong attention to detail Ability to manage multiple studies and competing timelines Tertiary qualification in health, science, or a related field Why Apply? Join a collaborative, purpose-driven clinical research environment Play a key role in accelerating trial delivery and patient impact Gain exposure to a variety of sponsors and study types Click Apply or contact Jo Turner, Divisional Manager, jturner@hpgconnect.com for a confidential discussion
