Overview

Reference Number: JO-1912-442047
Principal Regulatory Writer
Rate: Negotiable
Job Type: Permanent
Location: Macclesfield

Principal Regulatory Writer Required

I am currently working with an established independent agency, with great expansion plans for 2020. Due to business demand within large regulatory projects, they are looking for an experienced Principal Regulatory Writer to join their reputable team due to continued success and growth.

With offices based in Cheshire, they are looking for someone to be either officed based or also have the flexibility for the ideal candidate to work fully remotely. You will benefit from great development opportunities, excellent remuneration and the chance to work with a company that really care.

You must have the following experience:

Ability to lead the planning and delivery of regulatory submissions and other large regulatory projects
Prepare clinical regulatory documents in a diverse range of therapy areas for their pharmaceutical clients
Drug-development experience, relevant to the field of regulatory writing
Clinical development and ICH guidelines for regulatory documents.
Authored a range of regulatory documentation including common technical document (CTD) modules, and regulatory briefing and response documents.
Strong scientific background, including a minimum of a BSc (or equivalent)

This is a fantastic opportunity to work with a company who invest, develop and progress their employees and really value those within.

Interviews for this role are taking place immediately, to be considered for this position please call Mark Watling on 01189 522 792 or alternatively email mark.watling@medcommsprofessionals.com .

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