Regulatory Affairs Project Manager: A succesful UK Pharma with specialist therapeutic areas offering Regulatory Affairs Project Manager role for an experienced Regulatory Affairs professional with solid RA background with EU submissions and CTA's. Project Manage and Line Manage the Regulatory Affairs team.
Title
Regulatory Affairs Manager / Regulatory Affairs Senior Manager / Senior Regulatory Affairs Manager / Regulatory Affairs Professional
Location
A1, A14, M11, Cambridge, Peterborough, Harlow, Bedford, Colchester, Ipswich, Chelmsford, Northampton, Corby, Kettering, KIngs Lynn, KIng's Lynn, Norwich, Colchester
Client
A succesful, growing UK Pharma based in Cambridgeshire, concentrating on a specialist therapy area. Work closely with teams in multiple offices.
Duties
As Senior Regulatory Affairs Submissions Coordinator you will report to the Regulatory Affairs Manager, key responsibilities will include:
•Management and maintenance of timelines for regulatory submissions
•Managing and training for the team for essential documentation throughout clinical trials
•Management of reviews, documentation and organisation of TMF
Experience
•Pharmaceutical research experience in Regulatory Affairs
•Experience managing CTA submissions
•European Regulatory experience
•Fluent in English
•Eligible to work in Europe
•Life Science degree
Salary and Benefits
£33,000 - 43,000 + benefits + bonuses based on experience
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 via LinkedIn: http://uk.linkedin.com/in/craigedwardsmeet
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@meet_craig
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