Regulatory Affairs Senior Manager


Competitive

REF: CRP484

Are you an experienced Regulatory Affairs professional looking for a Senior position in a specialist Pharmaceutical company? Do you have a strong working knowledge of US and EU regulations?

Key Information

  • London
  • 01423 813520
  • Full-time, Permanent
  • 10-07-2020
  • Competitive
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Job Description

The opportunity has arisen for an experienced RA professional to join an innovative US-based pharmaceutical organisation. This position offers invaluable experience to co-ordinate compliance activities surrounding a multitude of therapeutic candidates at different stages of product development.

You will be based at our client’s London office, acting as the regulatory expert for all activities up to commercialisation. Your knowledge and guidance will be paramount in progressing products through the pipeline. You will be responsible for the preparation and review of submission documents, including Market Authorisations and clinical trial applications.

You must be an excellent communicator, acting as the company’s interface with contractors, partners and external stakeholders, offering advice and assistance where appropriate. You will also work directly with global regulatory authorities to ensure all projects are compliant to the necessary guidelines.

In return you shall receive a competitive salary, a range of company benefits and the opportunity to play a major part in the development of several exciting products.

For more information or to apply, please contact Chris Vinter on 01423 813520 or alternatively send your CV to chris.vinter@networkscientific.co.uk.

Please note that all applicants for this regulatory affairs job should be able to prove that they are legally entitled to work in the UK. Network Scientific Recruitment, part of Network Scientific Ltd. is an Employment Business/Agency.

To be considered...

The successful candidate will have substantial Regulatory Affairs experience relating to the development of drug-device combinations. You will have worked on multiple projects and been integral in all aspects of the pre-approval process. A solid working knowledge of US and EU medical device submission regulations is essential.

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