Director of Regulatory Affairs - Reading, Berkshire, United Kingdom - Blackfield Associates

Description

Job Description

Our client, a pharmaceutical development company has a requirement for a Regulatory Affairs Director to join their UK team. This role is perfect for a senior manager/ experienced regulatory professional who is looking to head up Strategy implantation with focus of the UK and EU market in medicinal products.

As Regulatory Affairs Director, you will:

• regulatory affairs expertise to projects seeking regulatory strategic input to their development programmes.
• Commercial and Marketing team to support company growth including client pitches, input into proposals, social media activity and Conferences
• development company capabilities in regulatory strategy.
• facing, expanding commercial offering/ project scope
• UK, and US are the geographical regions of key focus

To be considered for the role of Regulatory Affairs Director, you will have:

• to degree level in related Life science field
• Least 8 years Regulatory experience, gained in a strategic, pharmaceutical development or high visibility position, providing oversight and input to drug development regulatory activity
• direct line management experience
• to advise clients on a strategic level covering a broad range of product development stages, geography, therapy areas and products.
• leadership and interpersonal skills.
• in a high visibility, guiding role and speaking to external stakeholders