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ARM has an exciting new role for anyone looking to secure a new position within the field of Regulatory Affairs. The role in questions is for a CMC Associate to work on a 12 month contract for a pharmaceutical prime at its office in Uxbridge; so with a central location, exciting product portfolio and development opportunities, this might be the right role for you.
The position is home based for the interim, however post COVID it will be office based in Uxbridge.
In this role, you will be provide product support to the CMC team on Module 3 work of regulatory submissions across phases of product development. Support may include organizing, managing and executing on regulatory CMC projects and submissions. Tasks may include creating and/or maintaining submission timelines and tables of contents, formatting of documents per style guide, scheduling meetings, drafting meeting agendas and minutes, managing document reviews and other tasks as requested. Ideal candidate has:
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