Company: Pharmalink Consulting
Closing Date: 07 Nov 16
Salary (£): Competitive
Genpact Pharmlink is a highly specialized Regulatory Affairs Consultancy with a successful history. We have grown and developed our service offering through building relationships, listening to our clients’ needs and adapting our ways of working to meet the changing needs of regulatory markets around the world. It is this flexibility and adaptability that we look for in all of our Consultants.
Role based – Maidenhead
Contract – 3 month contract
Specialisation – CMC, regulatory documentation dossier review
Scope of the role:
Genpact Pharmalink Global Regulatory Affairs combines Pharmalink’s domain expertise in consulting, project support and outsourced regulatory affairs services with Genpact’s global delivery, BPO, technology and analytics offerings for the global life sciences market.
Accountabilities & Role requirements:
• Dossier review
• Looking for a regulatory consultant with at least 2-3 years experience
• Regulatory consulting and supporting expertise
• Experience with Regulatory CMC
• Requirement to attend training oversees.
Vanwall Business Park
|Tel:||+44 (0) 1628 860300|
|Fax:||+44 (0) 1628 860400|
|Website:||Visit Our Web Site|
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