Benefit Risk Evaluation Assessor

Medicines and Healthcare products Regulatory Agency, Poplar, Greater London

Benefit Risk Evaluation Assessor

Salary not available. View on company website.

Medicines and Healthcare products Regulatory Agency, Poplar, Greater London

  • Full time
  • Permanent
  • Onsite working

Posted 1 week ago, 26 Jun | Get your application in now before you miss out!

Closing date: Closing date not specified

job Ref: 2e2cdd1b4a5d4a4b9e8af87790489f5a

Full Job Description

Benefit Risk Evaluation Assessor

Employer
Medicines & Healthcare products Regulatory Agency

Location
London Canary Wharf/Hybrid

Salary
£73,324 per annum plus benefits

Start date
24 Jun 2025

Closing date
14 Jul 2025

Discipline
HEOR, Analyst, Outcomes, HR / Recruitment / Training

Hours
Full Time

Contract Type
Permanent

Experience Level
Senior Management

The MHRA is transforming. Through enabling innovation, making the right judgements of the benefits and risks of medical products and forging the right partnerships in the UK and internationally, it aims to deliver world class regulation and improved outcomes for UK patients.

We are currently looking for an experienced Benefit Risk Evaluation Assessor to join our Benefit Risk Evaluation II team in the Safety and Surveillance group.

Within a week of working here, your day could look like this: to provide a robust benefit risk assessment of potential safety signals within the Musculoskeletal, Trauma and Cosmetic therapeutic area using data from a range of sources and technical, scientific, clinical and regulatory knowledge and/or practical experience. Benefit risk assessors are responsible for engaging with a range of stakeholders including patients and the public to make timely and robust benefit-risk assessments and recommend safety actions and risk mitigations that are outcome focused.

The successful candidate will help deliver on our ongoing work and increase capacity to respond to new-emerging safety issues. They will have comprehensive medical device regulatory experience as well as professional, technical or scientific expertise in the Musculoskeletal, Trauma and Cosmetic therapeutic area.

  • Have comprehensive experience in critically analysing clinical/scientific information from a range of sources including case reports, registries, clinical trials/investigations, and observational studies, making sound judgements for recommendations to protect patient safety and public health.
  • Have in depth knowledge and experience of relevant regulations and procedures applicable to medical devices.
  • Have previous therapeutic and/or technical experience and expertise relevant to the work of the Musculoskeletal, Trauma and Cosmetic Benefit-Risk Evaluation team.
  • Have excellent interpersonal skills to facilitate team-working/team-leading, consulting and co-operating with colleagues from different disciplines and with variable degrees of expertise.
  • Share knowledge to improve the capability of the team, benefit risk evaluation group and the wider safety and surveillance function.

Closing date: 14 July 2025


#s1-Gen

The successful candidate will help deliver on our ongoing work and increase capacity to respond to new-emerging safety issues. They will have comprehensive medical device regulatory experience as well as professional, technical or scientific expertise in the Musculoskeletal, Trauma and Cosmetic therapeutic area.
  • Have comprehensive experience in critically analysing clinical/scientific information from a range of sources including case reports, registries, clinical trials/investigations, and observational studies, making sound judgements for recommendations to protect patient safety and public health.
  • Have in depth knowledge and experience of relevant regulations and procedures applicable medical devices.
  • Have previous therapeutic and/or technical experience and expertise relevant to the work of the Musculoskeletal, Trauma and Cosmetic Benefit-Risk Evaluation team.
  • Have excellent interpersonal skills to facilitate team-working/team-leading, consulting and co-operating with colleagues from different disciplines and with variable degrees of expertise.
  • Share knowledge to improve the capability of the team, benefit risk evaluation group and the wider safety and surveillance function.

    The MHRA is transforming. Through enabling innovation, making the right judgements of the benefits and risks or medical products and forging the right partnerships in the UK and internationally, it aims to deliver world class regulation and improved outcomes for UK patients.

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