Regulatory Submissions Publisher

Exciting Regulatory Submissions Publisher opportunity at one of the world’s leading Pharma companies!

They are looking for a Regulatory Operations professional with extensive experience with Publishing Regulatory submissions to join their team as a Regulatory Submissions Coordinator!

The key responsibilities of this regulatory role include:

• Performing submission publishing activities in eCTD and non-eCTD format across US and countries within the EMEA-Emerging Markets (EM) region
• Using current electronic document management and publishing tools to assemble, publish, validate, and dispatch dossiers
• Performing QC of electronic and paper submissions to ensure compliance with HA and internal requirements, guidelines, and processes

We’re looking to speak with any candidates that have:

• A minimum of 2-4 years of experience required in the pharmaceutical industry or related experience
• Experience using Liquent Insight Publisher and ISI Publisher tools
• Experience working on submissions for US and EMEA regions

This Regulatory Publishing opportunity is an initial short-term contract, which is offering an extremely competitive rate for the right candidate. This is a 100% remote-based role, with the offices based in Europe.

If you have read this through and believe you would be a great fit for this Regulatory Operations position, please do not hesitate to apply, or simply reach out to me via email bshepherd@aerotek.co.uk, or just send me a message so we can schedule a call to discuss it further!

If this does not sound like the right role for you but you know someone that could be right for a Regulatory management position, please forward on a method of contact to this person and you could be eligible of a referral fee.