Regulatory Specialist, Study Start-Up

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