Job title: Senior Manager, Global Regulatory Affairs - Neurology

A global Pharmaceutical business with offices in Hertfordshire are seeking a Global Senior Regulatory Affairs Manager to support European Regulatory activities for an exciting Neurology pipeline. This role will act as the EU Regulatory Lead for a specific area within the Neurology pipeline and will input into global regulatory strategy and support the design of clinical development programmes.

Responsibilities:

• Involvement in post-approval activities for centralised procedures
• Supporting global regulatory strategy
• Responsible for designing clinical development programmes
• Collaborating with cross-function teams in the UK, US and Japan
• Lead the preparation of an Orphan drug application, PIP and clinical trial application

Requirements:

• Experience within EU and UK regulatory processes is essential
• Minimum of 4 years' experience within Pharmaceutical Regulatory Affairs
• Full product lifecycle experience as a minimum
• Experience working within a Neurology portfolio is desirable
• Experience working within Paediatrics is desirable

Salary and benefits:

A competitive basic salary, car allowance, annual bonus, pension and healthcare plan are on offer

To apply for this position or hear further details then please contact Matt Thomas via matt.thomas@pharma-partners.co.uk