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Job summary

Main area
Pharmacovigilance
Grade
NHS AfC: Band 6
Contract
8 months (Fixed Term - Until November 2027)
Hours
Full time - 37.5 hours per week
Job ref
282-CR1966
Employer
The Royal Marsden NHS Foundation Trust
Employer type
NHS
Site
The Royal Marsden Hospital Sutton
Town
Sutton
Salary
£45,953 - £54,254 per annum
Salary period
Yearly
Closing
13/11/2026 17:00
Interview date
30/11/2026

Employer heading

The Royal Marsden NHS Foundation Trust logo

Pharmacovigilance Officer

NHS AfC: Band 6

Job overview

A Pharmacovigilance (PV) Officer (maternity cover) is required to assist managing sponsor oversight activities around the safety aspects of clinical trials and other clinical studies. The PV Officer will be part of the GCP & Regulatory Compliance Team, which ensures RM/ICR fulfil the extensive UK legislative requirements for conducting clinical research projects (and other overseas requirements, where applicable). 

Main duties of the job

Candidates will be required to have experience working to GCP standards and have experience also in pharmacovigilance. If the successful candidate is an internal applicant, the role will be offered as a secondment - please note line management approval must be obtained before applying. For external candidates, the position is offered on a fixed-term basis.

The Trust recognises that candidates may use artificial intelligence (AI) tools during the application process. Whilst these may be used for drafting, applicants remain wholly responsible for the accuracy, authenticity and truthfulness of all the information submitted. Applications or interview responses that include false, misleading, or unverifiable content (generated by AI or otherwise) may lead to withdrawal from the recruitment process.

Working for our organisation

The Royal Marsden NHS Foundation Trust is a world-leading cancer centre. Our role is to offer our patients the best cancer care available anywhere in the world, and to continue to make a global contribution to finding better ways of diagnosing and treating cancer. We employ over 4,500 staff in a diverse range of careers including nursing, medical, science, radiography, pharmacy, occupational therapy, finance and administrative services. We have two hospitals – one in Chelsea, London, and one in Sutton, Surrey – as well as a Medical Daycare Unit in Kingston Hospital.

At The Royal Marsden, we deal with cancer every day, so we understand how valuable life is. When people entrust their lives to us, they have the right to demand the very best. That's why the pursuit of excellence lies at the heart of everything we do.

At the heart of the hospital is our dedicated team. We offer a stimulating and dynamic working environment, a wide range of staff benefits, learning and development opportunities and clear career pathways. There are opportunities to work flexibly across a range of areas and specialities and we welcome flexible working requests from point of hire to support employees work life balance. We are looking for employees who aspire to excellence, share our values and can play a crucial role in our on-going achievements.

Detailed job description and main responsibilities

For further information on the role please refer to the job description and personal specification

  • To provide support and expert advice to clinical research teams in developing pharmacovigilance sections of new clinical trials protocols.
  • To assist in the reporting of SUSARS and Serious Breaches to the MHRA and REC. 
  • To monitor pharmacovigilance processes (including for example hosted and sponsored USMs) and their reporting, and escalating issues when required.
  • Co-ordinate and perform pharmacovigilance audits in preparation for Developmental Safety Update Reports (DSURS) production and submission.
  • To co-ordinate and assist in the production and submission of Developmental Safety Update Reports (DSURS) to the MHRA.

Person specification

Education/Qualifications

Essential criteria
  • Degree in a life sciences or related discipline or equivalent experience in clinical research
  • Recognised GCP training
Desirable criteria
  • Degree or post-graduation in pharmacy, pharmacology, or related drug safety qualification
  • Evidence of completion of pharmacovigilance course(s) with a reputable provider e.g., MedDRA coding training certificate from MSSO

Experience

Essential criteria
  • Experience of working to UK Clinical Trials Regulations in an administrative role
  • Experience of working in a quality assurance / audit / monitor / pharmacovigilance / trial management role within clinical research
  • Ability to read and understand clinical research protocols and associated research documents, and to critically evaluate them
  • Experience of working in the NHS or relevant clinical / research environment (with non-commercial clinical trials and studies)
  • Proven ability to develop effective working relationships and to resolve data / quality / operational issues collaboratively
  • Awareness of Adverse Events reporting requirements for CTIMPs, non-CTIMPs and CIMDs
Desirable criteria
  • Experience preparing, evaluating, and submitting Development Safety Update Reports (DSURs)
  • Experience preparing, evaluating, and submitting Individual Case Safety Reports (ICSRs)
  • Experience of developing practical, proportionate data-collection tools and processes to evaluate quality and compliance

Skills, Abilities and Knowledge

Essential criteria
  • Ability to work in a proactive manner to identify new risks and issues, and flag these upwards appropriately
  • Ability to work on own initiative, and comfortable working independently and collaboratively as part of a diverse team
  • Proven ability to organise own work in busy work environment and time critical situations
  • Excellent administrative and organisational skills with high level of accuracy and attention to detail
  • Ability to summarise and explain complex issues to both technical and non-technical audiences both in written form and through presentations
  • Excellent IT skills including Microsoft Office Suites
  • Flexible to meet the needs of the service (e.g., working ad hoc to support regulatory inspections)
  • Able to work on both RM sites and to be flexible to meet the needs of the role

Employer certification / accreditation badges

Trust IDApprenticeships logoLondon Living Wage is a voluntary commitment made by employers, who can become accredited with the Living Wage FoundationArmed Forces Covenant Gold AwardDisability confident employerCare quality commission - OutstandingStep into healthMenopause Friendly 2025

Documents to download

Apply online now

Further details / informal visits contact

Name
Jefferson Lisboa Santos
Job title
Senior Pharmacovigilance Officer
Email address
[email protected]
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