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Senior Regulatory Consultant

Business Type: Clinical Research Organisation
Job Type: Clinical Research, Clinical Study- Trials, Regulatory Affairs
Job Level: Not Specified
Position: Full Time
Salary: Competitive
Location: East Anglia
Reference: 17527/002
Closing Date: 10/07/12
Our Client offers a wide range of support services to the global healthcare industry; from high-end strategic thinking and research to internal and external communications. They are currently seeking a Senior Regulatory Consultant for their Cambridge office.

Providing expertise, lead and deliver work programmes within the areas of, regulatory affairs, drug safety or risk management
Negotiate business with clients and write discussion documents and proposals
Monitor resource, budget and delivery requirements
Liaise ref programme costings and budgets, and client invoicing
Client account development
Maximise new work opportunities (programme development and new leads)
Development of innovative new services
Team management and development

Science Degree plus commercial acumen gained through either a pharmaceutical role and/or consultancy or agency environment
Experience of providing support to pharmaceutical drug development
Demonstrable record of project delivery, business development and a new service offering development in the consultancy area
Demonstrable success in winning new consultancy projects and/or evidence of thought leadership in drug development in either regulatory affairs, drug safety or risk management

Computer literacy; ability to use Microsoft Office (Word, PowerPoint, Outlook, Excel, Project)
Superior presentational skills; ability to deliver with clarity and confidence
Interpersonal skills; ability to communicate with people at all levels, negotiate and lead

Fforde is acting as a recruitment agency/business.

KEY WORDS: Senior Regulatory, Drug Development, Drug Safety, Risk Management, Science, Pharmaceutical, Regulatory, Pharmaceutical, Cambridge

Posted: 12/06/2012 | NPJ Ref: 83047
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