Regulatory Affairs, Manager, Associate Director, Regulatory Submissions, Regulatory Agencies Representative, Regulatory Line Manager, AD of RA, Global Regulatory, Biotech, UK, England
This exciting client is a rapidly expanding American Biotech company with over twenty years of experience across cadriology, oncology and infectious diseases.
This position as Associate Director of Regulatory Affairs will offer you full responsibility for all EU Regulatory Submissions, global interaction, provide guidance to development teams and represent the company to Regulatory Agencies.
£65,000 - £75,000 + bonus + benefits
Office based- Surrey / Berkshire/ Buckinghamshire/ West Sussex/ Hampshire/
Working as the Associate Director / Manager of Regulatory Affairs your responsibilities will include:
•Guidance on regulatory decisions and agency interaction
•Strategy across regulatory submissions along scientific and technical reviews
•Represent the company with regulatory agencies
•Line management of EU regulatory staff – performance review, training and appraisals
To be successful in this process, you must have the following expertise:
•Background in Regulatory Affairs – ideally to manager or director levels
•8yrs+ in clinical, RA or QA ideal
•European or Global scope and responsibilities
•Previous line management experience beneficial
•Strong life sciences education
A fantastic role, ideal for a Regulatory Affairs Manager looking to take a step forward in their career. This new role will be sought after, so do not hesitate to call today!
Full company details and job description are available upon application; no CV is submitted until full discussion has taken place. Please contact Craig Edwards at Meet on +44 203 178 7488 or email craig@peoplewithchemistry.com
Contact me via LinkedIn at the following link: http://uk.linkedin.com/in/craigedwardsmeet
Find out more about Meet at www.peoplewithchemistry.com
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