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Senior Regulatory Affairs Consultant - Labelling (home or office based)
Senior Regulatory Affairs Consultant - Labelling (home or office based)Parexel • Oxnard, CA, US
Senior Regulatory Affairs Consultant - Labelling (home or office based)

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

Parexel • Oxnard, CA, US
[job_card.30_days_ago]
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  • [job_card.full_time]
[job_card.job_description]

European Labelling & Promotional Regulatory Specialist

When our values align, there's no limit to what we can achieve. At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.

Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.

About the Role

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.

Key Responsibilities

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
  • Qualifications & Skills Required for the Role :

  • 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
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