Senior Regulatory Affairs Consultant Location: UK BASED (covering Asia Pacific, Latin America, Central & Eastern Europe) Company: Global Biopharmaceutical Leader Your new company This is an exciting opportunity to join a leading global biopharmaceutical company, renowned for its innovation in neurological and rare disease therapies. You'll be part of a high-performing regulatory team supporting product expansion across 70 international growth markets. Your new role As a Senior Regulatory Affairs Consultant, you will lead regulatory submissions for 1-3 products across Asia Pacific, LATAM, and Central & Eastern Europe. You'll be a key member of the global regulatory project team, collaborating closely with the Global Regulatory Lead (GRL) and cross-functional partners in medical writing, pharmacovigilance, clinical, and CMC. You'll oversee the operational work of a CRO, ensuring timely and compliant submissions, and play a central role in implementing regional regulatory strategies aligned with EU, US, and Swiss standards. The role also includes lifecycle management (LCM), core data sheet (CDS) compliance, and managing readiness-to-questions (RTQs). Familiarity with Veeva Vault is a plus, as the platform is being introduced. What you'll need to succeed Strong regulatory affairs experience across international markets Extensive strategic regulatory experience for LCM products Deep understanding of global regulatory frameworks (EU, US, Swiss) Experience managing CROs and cross-functional collaboration Excellent communication and stakeholder engagement skills Proven ability to lead product submissions and lifecycle activities Knowledge of Veeva Vault is advantageous. What you'll get in return Opportunity to lead high-impact regulatory projects across diverse global markets 12-month contract with scope to extend up to 3 years Work with a respected biopharma company on innovative therapies Collaborate with global experts in a supportive, cross-functional environment Competitive compensation and flexible working arrangements 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. ADZN1_UKTJ