Senior Regulatory Affairs Consultant - Labelling; or office based

Senior Regulatory Affairs Consultant - Labelling (home or office based)

Parexel, Uxbridge, England, United Kingdom

We are seeking an experienced Regulatory Affairs professional to join our team as a European Labelling & Promotional Regulatory Specialist. This key position provides expert guidance across a Therapeutic business unit, delivering both strategic and operational regulatory input to cross-functional teams. The role can be home or office based in various European locations.

• EU Product Information Management: Create, update and maintain EU Product Information in line with CCDS, Agency RTQ, and current labelling requirements. Serve as the key point of contact for EU Product Information for both internal and external stakeholders. Lead reviews, round tables, and approvals for EU Product Information in appropriate systems according to SOPs. Deliver competitive labelling searches and contribute to TCLP for early development assets.
• Operational Excellence: Ensure timely tracking and management of all EU Product Information in appropriate systems. Lead Readability Testing processes including vendor selection, agreement management, questionnaire review, and submission of final reports. Coordinate Linguistic Review processes with LR Coordinator according to SOPs. Communicate proactively with SPA for artwork and mock-up changes, participating in Change Control Processes.
• Leadership &
  
  Collaboration:
  
  Lead the Local Labelling Committee for creation, review and approval of EU Product Information. Serve on the EU Clearance Committee as primary regulatory reviewer for promotional materials. Build strong relationships with EU and Global Regulatory teams, local business partners, SPA, and PLG teams. Monitor changes in EMA labelling requirements and keep the organization informed of technology requirements.

• University degree in a life science discipline
• Strong knowledge of EU regulatory requirements for product labelling and promotional materials
• Experience with electronic content management systems and regulatory SOPs
• Excellent project management and organizational abilities
• Outstanding written and verbal communication skills
• Proven ability to work effectively in cross-functional teams
• Fluent in English, written and spoken

• Mid-Senior level

• Full-time

• Research and Consulting

• Pharmaceutical Manufacturing
• Biotechnology Research
• Hospitals and Health Care

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