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Vacancy details
Vacancy description:
Job Code:
1052
Job Title:
Regulatory Affairs Manager
Job Category:
Regulatory And Drug Safety
Contract:
Permanent
Discipline:
Regulatory Affairs
Country:
United Kingdom
Location:
Any Location
Min experience:
N/A
Annual salary:
Negotiable
Apply by:
30 Nov 2008
JOB SUMMARY
Regulatory Affairs Manager required by innovative Pharmaceutical Company based in the North-West of England (Liverpool/Manchester area).
The company is part of a major group employing 16,500 people globally. You will be joining their exciting Healthcare division focused on pharmaceutical medicine.
Key Responsibilities
Responsible for coordination of regulatory submissions and for communicating with the regulatory authorities in the UK, Europe and the USA for all issues associated with company’s expanding drug development pipeline.
Review all documentation required for regulatory submissions
Line management
Benefits
Competitive Salary
Car Allowance
Pension
Healthcare
Life Assurance
Friendly and welcoming working environment
Ongoing training & development
Qualifications
Life Science Degree
5+yrs in Regulatory Affairs
Experience as a Regulatory Affairs Manager
Thorough knowledge of European and USA (FDA) Regulatory Guidelines
Excellent understanding of the drug development process
To Apply
i-Pharm Consulting is a specialist recruitment company focused on mid to high-level roles in Clinical Research & Medical Affairs. We recruit for both permanent and contract staff across the UK & Europe. Our clients include Pharmaceutical, Biotechnology, Contract Research and Medical Device companies
About i-Pharm Consulting
If you would like to discuss this vacancy further please submit your CV using the button below OR call Senior Consultant David Hendron on +44 (0)20 3189 2299.
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