Overview

Reference Number: JO-2209-501879
Senior Regulatory Consultant
Rate: Negotiable
Job Type: Permanent
Location: Hertford

Senior Regulatory Consultant / Principle Regulatory Consultant

Location: Hertfordshire

Salary: Flexible dependent on experience

Benefits: Home working, Pension scheme, Healthcare, Life assurance and more

Permanent position

Reference number: JO-2209-501879

An award winning Regulatory consultancy who provide expert services to pharmaceutical and biotech companies are recruiting for an experienced Regulatory Affairs Professionals. The ideal candidate will have strong experience in early phase development, however given the nature of our client’s requirements, they are willing to consider any applicants with broader regulatory knowledge. This client would like a rounded Candidate and as such will look for candidates with good knowledge of CTAs, new MAAs and further to post approval activities.

Responsibilities

• Managing submissions for products going through development and post marketing activities

• Will work across MAA’s, CTA’s, preparing documents for Scientific Advice, PIPs

• Writing/Reviewing variations and submissions

• Coordinate all post approval activities

• Coordinate regulatory activities for the EU markets

Requirements

• EU regulatory experience is essential

• Early or Late phase Drug Development experience

• Ability to work under pressure and achieve timely submissions

• ATMP knowledge advantageous

• Innovative Product Background essential

If you are interested in this role please email your CV to george.eyre@cpl.com or call George Eyre on 07787604445

Remember if this role is not suitable for you please feel free to forward this to anyone you feel would be suitable. If we successfully find a role for your recommendation we will offer vouchers of your choice up to the value of £250.