The role You’ll own regulatory activities from study selection through site activation, working closely with business development, patient recruitment, site leadership and quality and compliance. What you’ll do • Manage regulatory submissions and documentation for new studies across multiple research sites • Coordinate proactively with business development and operational teams to keep study start-up on track • Maintain accurate, inspection-ready regulatory files • Spot risks and bottlenecks early and propose practical solutions • Help refine and improve start-up processes as the team scales About you • Prior regulatory or study start-up experience within a clinical research site network, ideally one of similar scale and pace • Excellent organisation and exceptional attention to detail • A strong sense of urgency and a track record of delivering high-quality work to deadlines • Strategic, analytical thinking: you connect the dots and don’t just execute tasks • Confident working independently and communicating clearly with remote, cross-functional teams