Regulatory Affairs Specialist

10 hours ago

London, Greater London, United Kingdom Cpl Healthcare Full time
Senior Regulatory Affairs Consultant - Submissions Manager

Are you a seasoned Regulatory Affairs professional looking for a new challenge? Do you have experience in planning, dispatch, submission, and approval of data packages to Regulatory Authorities? We have an exciting opportunity for a Senior Regulatory Affairs Consultant - Submissions Manager to join our team at Cpl Healthcare.

This role is ideal for someone who is passionate about regulatory affairs and has a strong understanding of regulatory legislation in the pharmaceutical industry. As a Senior Regulatory Affairs Consultant - Submissions Manager, you will be responsible for:

Key Responsibilities:
  1. Preparing documents for regulatory dossiers/data-packages to meet submission timelines.
  2. Managing vaccine registration activities for one or several projects, identifying key issues that could prevent achieving objectives and proactively addressing them.

We are looking for someone with a university degree in a relevant field, ideally with more than 3 years of experience in the pharmaceutical industry. Knowledge of regulatory legislation in at least one geographic area is essential.

This role offers a competitive salary, a 15% bonus, and a £5,760 car allowance, as well as a range of other benefits. If you are a motivated and experienced Regulatory Affairs professional looking for a new challenge, please apply today.

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