Full-Time

Medical Assessor

Posted on 10/1/2025

Deadline 10/19/25
MHRA

MHRA

1,001-5,000 employees

Regulates medicines and medical devices

No salary listed

London, UK

Hybrid

Minimum of 8 days per month working on site, with potential to flex up to 12 days.

Category
Medical, Clinical & Veterinary (1)
Required Skills
Data Analysis
Requirements
  • Degree in Medicine and with a relevant postgraduate qualification within specialist area.
  • Registered with the General Medical Council.
  • Clinical, academic or pharmaceutical medicine experience, including evidence of analysis of data and preparation of reports, scientific publications or regulatory submissions.
  • Excellent interpersonal skills to facilitate team-working/team-leading, consulting and co-operating with colleagues from different disciplines and with variable degrees of expertise.
  • Evidence of an up-to-date specialist level knowledge in one or more relevant scientific areas.
Responsibilities
  • Carry out the assessment of clinical data provided in marketing authorisation initial and variation applications and/or paediatric data from various sources, including data with new, wide-ranging, or complex issues, making appropriate recommendations and decisions aligned with the protection of public health.
  • Manage own workload working in conjunction with other assessors to meet agreed timelines responding to public health demands.
  • Prepare present and discuss objective assessments or other scientific papers at expert advisory groups, e.g., Commission on Human Medicines as needed.
  • Take a lead in providing reliable, timely and appropriate scientific and regulatory advice to companies and in writing reflecting contemporary regulatory guidance and relevant regulatory decisions.
  • Mentor or coach other staff to enhance their knowledge and contribution.
  • Provide advice to colleagues in the division or Agency as needed.
  • Contribute to and influence assessment policy and practice, and proactively identify where such contributions would be beneficial.
  • Contribute to and influence divisional procedures.
  • Make individual contributions to representational or professional activities inside or outside the Agency.
  • Support and develop interactions with international regulators, both for assessments and regulatory science.
  • Develop good working relationships with colleagues and with internal and external stakeholders.
  • Deal effectively with official correspondence to agreed timelines.
Desired Qualifications
  • Managing a Quality Service
  • Deliver at Pace
  • Communicating and Influencing

MHRA is an executive non-departmental public body responsible to the Secretary of State for Environment, Food and Rural Affairs. Its purpose is to protect and improve England’s natural environment and to encourage people to enjoy and get involved in their surroundings. It carries out policy implementation, land stewardship, conservation funding, and public engagement through government-backed programs and partnerships with landowners, communities, and volunteers. Its goal is to safeguard natural spaces, biodiversity, and landscapes while inviting people to participate in caring for and enjoying the environment.

Company Size

1,001-5,000

Company Stage

N/A

Total Funding

N/A

Headquarters

London, United Kingdom

Founded

1989

Simplify Jobs

Simplify's Take

What believers are saying

  • Flexible wildlife licensing for infrastructure projects balances conservation with necessary development.
  • Evidence-based standards and partnerships target 30x30 nature recovery and species decline halt.
  • Green infrastructure integration through spatial planning delivers combined environmental and community benefits.

What critics are saying

  • 20% MHRA workforce reduction undermines regulatory capacity and clinical trial oversight.
  • Only five operational Approved Bodies create bottlenecks for Class III device conformity assessments.
  • Post-Brexit regulatory divergence forces UK medtech firms into separate UKCA marking processes.

What makes MHRA unique

  • MHRA independently regulates UK medicines, vaccines, and medical devices post-Brexit.
  • Three-year Strategy for Improving Safety Communications transforms patient and healthcare professional engagement.
  • New regulations effective April 28, 2026 align UK clinical trial oversight standards.

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Benefits

Flexible Work Hours

Hybrid Work Options

Remote Work Options

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