Medical Assessor
Greater London, London, Greater London, W1B, England, UK
Listed on 2026-07-09
-
Doctor/Physician
Overview
We are currently looking for a Medical Assessor to join our Innovative Medicines Function within the Health Quality and Access group.
This is a full-time
, permanent opportunity based at 10 South Colonnade, Canary Wharf London, E14 4PU
.
We are implementing a flexible, hybrid way of working, with a minimum of 8 days per month working on site to enable collaboration and contact with partners and stakeholders needed to deliver MHRA business. Attendance on site is driven by business needs so depending on the nature of the role, this can flex up to 12 days a month, with the remainder of time worked either remotely or in the office.
Some roles will need to be on site more regularly. Remote working is potentially available for some specific roles. Please discuss this with the recruiting manager before accepting an appointment.
Reporting to the Team or Function Manager in Innovative Medicines, the medical assessors are required to assess the clinical and regulatory aspects of initial and variation marketing authorisation applications for chemical or biological medicinal products, in a variety of therapeutic fields including those with new or complex issues for adult and paediatric patients.
Key responsibilities- Carry out the assessment of clinical data provided in marketing authorisation initial and variation applications
- Share Knowledge and Development of Self and Colleagues
- Contribute to Policy and Procedures
- Communicate with internal and external stakeholders
Oursuccessful candidate will demonstrate the following:
Qualifications- Degree in Medicine and with a relevant postgraduate qualification within specialist area.
- Registered with the General Medical Council and holding a licence to practise or eligible and willing to obtain/reactivate a licence to practise upon joining the Agency
- Ability to critically analyse clinical/scientific information from a range of sources including clinical trials and observational studies.
- Evidence of an up-to-date specialist level knowledge and experience in one or more relevant scientific areas. Experience in the field of immunology or oncology would be advantageous, but other specialist clinical areas also welcome.
- Ability to make independent decisions on the benefit-risk balance of medicines, supported by a clear rationale.
- Good knowledge of relevant regulations applicable the licensing of medicinal products
A=Application, T=Test, I=Interview, P=Presentation
Ability Criteria- Ability to critically analyse clinical/scientific information from a range of sources including clinical trials and observational studies. (A,I,T)
- Ability to make independent decisions on the benefit-risk balance of medicines, supported by a clear rationale. (A,I,T)
- Managing a Quality Service (A,I)
- Delivering at Pace (A,I)
- Communication and Influencing (A,I)
- Clinical, academic or pharmaceutical medicine experience, including evidence of analysis of complex data, decision-making, and preparation of comprehensive, authoritative reports, scientific publications or regulatory submissions (A,I)
- Excellent verbal and written presentation skills appropriate to the target audience including evidence of communication with patients and other members of the public, and expert medical groups and committees. (A,I)
- Excellent interpersonal skills to facilitate team-working/team-leading, consulting and co-operating with colleagues from different disciplines and with variable degrees of expertise. (A,I)
- Degree in Medicine and with a relevant postgraduate qualification within specialist area.
- Registered with the General Medical Council (GMC) and holding a licence to practise or eligible and willing to obtain/reactivate a licence to practise upon joining the Agency (A)
- Evidence of an up-to-date specialist level knowledge and experience in one or more relevant scientific areas. Experience in the field of immunology or oncology would be advantageous, but other specialist clinical areas also welcome. (A,I)
- Good knowledge of relevant regulations applicable the licensing of medicinal products (A,I)
Closing date: 23rd July 2026
Shortlisting date: from 1st August 2026
Interview date: from 1st September 2026
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