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  • Job type

    Contract
  • Location

    Slough (can be remote in UK)
  • Working Pattern

    Full-time
  • Specialism

    Regulatory Affairs
  • Industry

    Pharmaceuticals
  • Pay

    Competitive

12 MONTH STRATEGIC REGULATORY LABELLING CONTRACT | GLOBAL | REGULATORY AFFAIRS

Your new company

An innovative leader in medicine within the neuroscience therapy area is looking for a global labelling leader to join their team as a contractor.

Your new role

You will be joining a team of 4 as a Regulatory Labelling Lead consultant to create and implement strategies related to CCDS. As the global labelling lead, you will be responsible for driving the core labelling strategy to ensure quality and compliance for safe and effective use of products. You will be responsible for developing this strategy and leading the development and updating of the core labelling documents through implementation at local and regional level.


You will be responsible for leading the creation and management of documents throughout the product lifecycle, including the CDS, Global Patient Leaflet, and Target Label Profile (TLP). You will be responsible for leading a cross-functional product labelling team to reach decisions on core labelling matters. You will also be responsible for overseeing the distribution and tracking of CDS updates to ensure compliance with the EDMs/ Regulatory Tracking System.

What you'll Need to Succeed
  • You must have a minimum of 8–10 years labelling experience within global Markets.
  • Strategic labelling expertise
  • Extensive experience with CCDS
  • Right to work and live in the UK

What you'll get in return

A contract role with a great rate on offer, can be fully remote in the UK. Potential to extend. The team is a flat structure, so there is a big opportunity to make an impact in this role.

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 and reach out to Julia Bowden for more details.

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