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Remote Regulatory Affairs Senior Associate

Hays Specialist Recruitment Limited
Posted 9 hours ago, valid for 16 days
Location

Uxbridge, Buckinghamshire UB8 1DH, England

Salary

£72,000 - £86,400 per annum

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Contract type

Full Time

In order to submit this application, a Reed account will be created for you. As such, in addition to applying for this job, you will be signed up to all Reed’s services as part of the process. By submitting this application, you agree to Reed’s Terms and Conditions and acknowledge that your personal data will be transferred to Reed and processed by them in accordance with their Privacy Policy.

Sonic Summary

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  • A well-known biopharmaceutical company is seeking a Senior Regulatory Affairs Associate EU for a 12-month remote contract, with the possibility of extension.
  • The role involves supporting a Regulatory Affairs Lead on projects and products, focusing on executing regional regulatory strategies and managing clinical trial applications.
  • Candidates must have prior Regulatory Affairs experience in clinical trials and a working knowledge of EU regulations to be considered for the position.
  • The job requires monthly meetings in either Cambridge or Uxbridge offices, and is primarily focused on Clinical Trial activities such as initial applications and end of trial reports.
  • The salary for this position is competitive, and the company is looking for candidates with a minimum of several years of relevant experience.

Senior Regulatory Affairs Associate EU

Your new company

This well-known biopharmaceutical company is looking for an experienced Senior Regulatory Affairs Associate EU to join the team on a contracting basis. This is a 12-month contract job with scope for extension. This contract job is remote with the exception of meeting once per month in Cambridge or Uxbridge offices.

Your new role

As Senior Regulatory Affairs Associate EU, you will support a Regulatory Affairs Lead with assigned projects and products in order to execute the regional regulatory strategy and regional regulatory plans.As Senior Regulatory Affairs Associate EU you will prepare supportive documentation for regulatory deliverables, including the management of clinical trial applications. This contract job is focussed on Clinical Trial activities; initial applications, substantial modifications, end of trial reports, compiling documents and some archiving activities.

What you'll need to succeed

In order to be considered for this contract job, you must have prior Regulatory Affairs experience working in clinical trials and working knowledge of EU regulations.

What you need to do now

For more information on this or any other Regulatory Affairs contract jobs, please apply for this advert.If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.If this job isn't quite right for you, but you are looking for a new position, please contact us for a confidential discussion about your career.

Apply now in a few quick clicks

In order to submit this application, a Reed account will be created for you. As such, in addition to applying for this job, you will be signed up to all Reed’s services as part of the process. By submitting this application, you agree to Reed’s Terms and Conditions and acknowledge that your personal data will be transferred to Reed and processed by them in accordance with their Privacy Policy.