Your new company You will be joining a leading biopharmaceutical company dedicated to developing innovative therapies for patients with serious and life-threatening conditions. This company is renowned for its commitment to scientific excellence and patient-centric approach. Your new role As the EU Regulatory Lead, you will manage the regulatory strategy for a molecule with three related indications. Your responsibilities include: Leading EU regulatory activities for clinical trials and ensuring timely submissions. Collaborating cross-functionally to implement regulatory changes. Representing the EU regulatory team in cross-functional meetings. Supporting other programs in various development stages and post-approval activities. Aligning with Global and US Regulatory Leads for successful outcomes. What you'll need to succeed 10 years of experience in Regulatory Affairs In-depth knowledge and experience with EU regulatory requirements and procedures. A proven track record of developing, implementing, and communicating regulatory strategies. Excellent documentation skills to ensure high-quality and timely submissions. Experience with EU guidance and leading regulatory processes, particularly in clinical trials and Type II variation submissions. Global experience, including collaboration with US regulatory teams, is highly advantageous. In return, you will receive: 12-Month Contract with attractive rates Scope for extension past 12 months A hybrid flexible model, with opportunities for remote working in the UK. What you need to do now If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.If this job isn't quite right for you, but you are looking for a new position, please contact Julia Bowden for a confidential discussion about your career.