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