Regulatory Affairs-PM/Snr Consultant- Reg Submission Management

Regulatory Affairs Project Manager/Consultant with extensive regulatory operations experience and specific regulatory submissions management and publishing required.

I have a number of 12 month contract Opportunities for a Regulatory Affairs Project Manager / Senior Consultant with a proven track record in the Pharma/BioTech industry (ideally 10 years experience). The successful candidate should have experience in Regulatory Submission Management and Publishing Processes. Previous experience in Submission Management Systems is a MUST.

The ROLE:Working with staff at various levels to gain a complete understanding of the current environment in relation to current Regulatory Submissions Management and Publishing Process. The consultant will formulate a deficiency document highlighting weaknesses in the process, toolset and related while designing a path forward to remediate found deficiencies.

The role is based in Boston and the client is willing to assist with travel and accommodation COSTS which makes this a very attractive contract opportunity. If you are interested, please attach an up to date resume and I will be in touch.
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