Regulatory Affairs Professional

11 hours ago


Addlestone, Surrey, United Kingdom CTI Clinical Trial and Consulting Services Full time
Job Description

The successful candidate will have a proven track record of successful health authority interactions and a strong understanding of global regulatory aspects for CMC across multiple dosage forms (oral and parenteral). They will be responsible for managing preparation and review of global registration packages, defining and implementing regulatory strategies for global registrations, variations, and health authority responses, and overseeing global submissions.

In this role, you will work closely with stakeholders, including other RA functions, Technology Manufacturing, Quality Assurance, and Business Partners, to ensure timely compilation and compliance with established standards and SOPs.

The estimated salary for this position is around £80,000 per annum, depending on experience, and we offer a hybrid working model with a minimum of 2 days per week in the UK office.



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