Senior Regulatory Affairs Officer

Exciting Senior Regulatory Affairs opportunity at one of the world’s leading healthcare companies!

They are looking for someone with profound regulatory affairs knowledge to provide operational support to the Clinical Research team.

The key responsibilities of this regulatory role include:

• Preparing and/or reviewing regulatory submissions to support clinical trial and marketing authorization activities
• Acting as a Regulatory Team Leader on complex projects, which may include technical writing and/or may act as a Project Manager for a stand-alone project
• Undertaking detailed review and management of budgets related to projects
• Establishing individual relationships with clients to discuss regulatory issues

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

• 3+ years’ experience within regulatory affairs
• Extensive knowledge of the job area as well as wider knowledge of the regulatory/pharmaceutical industry
• Experience with clinical trial regulatory submissions
• Experience with writing high-standard regulatory and/or technical documents

This Regulatory Affairs role is a permanent position. The role is paying competitive salary and is flexible with their remote working requirements but do prefer some travel to the site in Reading.

If you have read this through, and believe you would be a great fit for this Regulatory Affairs position, please send your CV to bshepherd@aerotek.co.uk. If this does not sound like the right role for you but you know someone that could be right, please forward on a method of contact to this person and you could be eligible of a referral fee. Also, we have a variety of roles that could be of interest but might not be advertised due to NDAs so please do feel free to send over your profile and we will be in touch with relevant positions.