Regulatory Affairs Manager

2 weeks ago

Slough Berkshire, United Kingdom Verbatim Pharma Full time
Job Description

Regulatory Affairs - Clinical Trial Services - Hybrid Opportunity

Are you ready to advance your career with a leader in Clinical Services? Providing the opportunity to specialise in a niche area of a business who have 3 key divisions, providing exposure to an area of the pharmaceutical industry being directly involved in saving the lives of some of the most vulnerable patients in the world.

As part of our close-knit regulatory team of four, you'll dive into developing intelligence materials, creating regulatory plans, and offering project-based support. You'll need a solid grasp of EU directives, US CFR, and GMP/GDP regulations.

Why this role?

  • You can delve into a classic RA position, with a fantastic team of specialists
  • Opportunities to progress, learn new things in a fast paced environment
  • This businesses passion trumps any other, truly matching your work ethic and in an extremely patient focussed space
  • One of the biggest service provider of this specialist area

This is a unique opportunity to experience a wide range of responsibilities in a fast-paced industry. If you're passionate about clinical services and ready to contribute to a growing company, apply now and be a part of something big

Alternate Job Titles:

RA Manager / RA Specialist / Regulatory Affairs Specialist / Reg Affairs Specialist / QA Manager

Commutable Locations:

Watford / Maidenhead / High Wycombe / Amersham / Slough / Bracknell / Staines / Watford / Woking / London / Greater London / Reading / Hampshire / Surrey

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