Job Details

Job Summary:

This is great role for a company on the move. They have successfully grown their pipeline into what is widely recognized as one of the best in the industry for a company of this size. You will be working in an expansive role, covering early and late stage development projects, Centralised filings and lifecycle management of the company’s most successful products. Contact Theo Moore on 0207 801 3384 or email your CV in confidence to cv@advregulatory.com

Requirements:

Title:
Regulatory Affairs Manager – EU Role but gain Global Development exp. – Great chance to develop your career for an expanding Pharma

Location:
You will be working in a Central london, easily commutable from the surround areas of London.

Background:
This position would suit somebody with strong interpersonal skills who likes to feel part of a strong team and likes to work with the team to develop other team members skills and experiences. They would need to enjoy all aspects of Regulatory, including both development and maintenance activities, and be a steady worker who is willing to take on any projects and undertake any activity in order to achieve the teams objectives.

Duties (with some supervision):
Defines EU filing strategy (CP, MRP, DCP) identifying risks and issues.
Develop and deliver regulatory strategies in support of new product registrations, in line with commercial objectives.
Makes recommendations to Global Regulatory and drug development teams in order to shape the global strategy in line with regional /commercial objectives.
Supports the drug development strategy, defining options for scientific advice, creating briefing packages and co-ordinating and leading EU agency meetings.

Experience & Qualifications:
The ideal candidate would need to enjoy all aspects of Regulatory, including both development and maintenance activities, and be a steady worker who is willing to take on any projects and undertake any activity in order to achieve the teams objectives. To be successful in this role, it would be essential to have good verbal and written communication skills, negotiation skills, good understanding and experience in EU regulatory requirements.

TO APPLY:
If you wish to apply for this role please click below, or send your CV with a covering note to cv@advregulatory.com quoting reference number noted above. Alternatively to have a confidential discussion about this or other potential roles or career options call Theo Moore or Matt Greig on +44 0207 801 3384

About ADV Regulatory
Advanced Regulatory has operating since 2004. We are a recruitment business dedicated to the pharmaceutical industry, specialising in Regulatory Affairs, Quality Assurance, Clinical Development, Pharmacovigilance and Health Economics and Outcomes Research. We match professional candidates to the best permanent, contract and interim roles in the market.

Visit us at www.advregulatory.com

Key words: Regulatory, Regulatory Affairs, Reg Affairs, Regulatory Affairs Director, Regulatory Affairs Associate Director, Regulatory Affairs Senior Manager, Regulatory Affairs Manager, Regulatory Affairs Executive, Regulatory Affairs Officer/ Regulatory Affairs / EU Regulatory