Senior Regulatory Affairs Specialist

2 weeks ago


Slough, United Kingdom ClinChoice Full time

Are you a skilled regulatory professional looking for a new challenge? ClinChoice is seeking a Senior Regulatory Affairs Specialist to join our team in the UK. This is an exciting opportunity to work on global clinical trials and develop your expertise in regulatory submissions.

In this role, you will be responsible for leading regulatory submission activities, including planning, authorizing, reviewing, and coordinating submissions for studies managed by the clinical operations team. You will provide guidance on regulatory requirements and guidelines, as well as represent the regulatory department in strategy discussions.

The ideal candidate will have a minimum of 8 years of experience in regulatory affairs, with a focus on the clinical development phase. They should have extensive knowledge of global regulatory submission and approval processes, as well as strong communication and leadership skills.

We offer a competitive salary of £85,000 per year, excellent work-life balance, and opportunities for career growth within ClinChoice. If you are passionate about regulatory affairs and want to make a difference in the pharmaceutical industry, we encourage you to apply.



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