Looking to make your mark within the regulatory space at an large healthcare conglomerate?
I-Pharm has partnered with a rapidly expanding global cooperation that specialises in various therapeutic areas. This market leader is in a phase of exponential growth and as a result they are looking for a Regulatory Affairs Lead on a 12 Month Fixed Term Contract to join their team in Hatfield.
This market leader operates across the globe.
The role offers 2 days per week on site in Hatfield and will involve but not be limited to:
Direct experience with dealing with UK MHRA
Managing regulatory submissions throughout out the lifecycle process
Clinical trial / PIP / MAA and maintaining licensing through renewals
Ph I - IV - life cycle management to their role (early development through to maintenance of licences)
Timely and high-quality MAA submissions leading to timely approvals aligned to TPP Prepares responses to regulatory agencies questions and other correspondence.
As a Regulatory Affairs Lead, you will need:
Must have experience with Marketing Authorisations Applications
Minimum of 2 years of experience working in Regulatory MAA
Communications with UK MHRA
Graduate in pharmaceutical sciences or medicine, pharmacy, life sciences
Fluent in English, both written and spoken
What\'s on offer:
High chance to move into a permanent position (TBC)
Bonus
Competitive salary
If you have read this far, why not get in touch to find out the granular details of this role and the impressive benefits this organisation is willing to offer you to undertake this exceptional opportunity!