IVD Assessor — Regulatory Reviews for Clinical Trials

IVD Assessor — Regulatory Reviews for Clinical Trials

Full-Time 50000 - 60000 £ / year (est.) No working from home possible
Medicines and Healthcare Products Regulatory Agency

At a Glance

  • Tasks: Lead reviews of In-Vitro Diagnostics for clinical trials and support regulatory development.
  • Company: Join the Medicines and Healthcare products Regulatory Agency (MHRA) in London.
  • Benefits: Competitive salary, professional growth, and a chance to shape healthcare regulations.
  • Other info: Dynamic role with opportunities for leadership and impact in the regulatory landscape.
  • Why this job: Make a real difference in healthcare by ensuring the safety and effectiveness of diagnostics.
  • Qualifications: Master’s degree in a related field and experience in IVD policy.

The predicted salary is between 50000 - 60000 £ per year.

Medicines and Healthcare products Regulatory Agency (MHRA) is seeking two IVD Assessors to join the Clinical Investigations Function.

Based at 10 South Colonnade, Canary Wharf, London, the roles involve leading reviews of In‑Vitro Diagnostics used in clinical trials and supporting regulatory regulation development.

The successful candidates will have a Master’s degree in a related field, with experience in IVD policy and regulatory frameworks, and excellent communication and leadership skills.

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Medicines and Healthcare Products Regulatory Agency

Contact Details:

Medicines and Healthcare Products Regulatory Agency Recruitment Team

We think you need these skills to ace IVD Assessor — Regulatory Reviews for Clinical Trials

IVD Policy Knowledge
Regulatory Frameworks
Leadership Skills
Communication Skills
Clinical Trial Experience
Analytical Skills
Attention to Detail