Job Title
Associate Director Regulatory Affairs, Manager, Associate Director, Regulatory Submissions, Regulatory Agencies Representative, Regulatory Line Manager, AD RA, Global Regulatory
Location
Office based, commutable from South-East, Surrey, Berkshire, Buckinghamshire, West Sussex area, Uxbridge, M4 Corridor, M3, M25, Slough, Ascott, Bracknell, Woking, Guildford,
Client
The client is expert in dealing with cadriology, oncology and infectious diseases. An American Biotech company with a history spanning two decades.
Duties
- Guidance on regulatory decisions and agency interaction
- Strategy across regulatory submissions along scientific and technical reviews
- Represent the company with regulatory agencies
- Line manage EU regulatory staff – performance review, training and appraisals
Experience
- Regulatory Affairs background – manager or assocaite director level
- 8yrs+ experience in Reg Affairs or similar clinical career
- European or Global responsibilities
- Previous line management experience beneficial
- Life-sciences education
Salary
£75,000 - £85,000 + bonus + benefits
Keywords
Pharmaceutical, Biotech, Biotechnology, Biochemistry, CRO, Pharma, Pharmaceutical, Clinical, Clinical Regulatory Affairs, Associate Director, Director, Manager, Submissions, GRA, RA, Regulatory Affairs, Regulatory Submissions, Regulatory Manager, Regulatory Affairs Director, Regulatory Affairs Associate Director, Regulatory Line Management, UK, England, South-East, Surrey, Berkshire, Buckinghamshire, West Sussex area, Uxbridge, M4 Corridor, Slough, Ascott, Bracknell, Woking, Guildford,
Application process
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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