At a Glance
- Tasks: Assist in evaluating safety applications for medicines and medical devices.
- Company: Join the Medicines and Healthcare products Regulatory Agency, enhancing public health.
- Benefits: Enjoy a competitive salary, generous pension contributions, and flexible working options.
- Why this job: Make a real difference in public health while developing your scientific career.
- Qualifications: Degree in life sciences and strong analytical skills required.
- Other info: Dynamic work environment with opportunities for professional growth.
The predicted salary is between 32617 - 36400 Β£ per year.
Details
Reference number
Salary
Β£32,617
A Civil Service Pension with an employer contribution of 28.97%
GBP
Job grade
Executive Officer
Contract type
Fixed term
Length of employment
12 months
Business area
MHRA β Safety and Surveillance Group
Type of role
Science
Working pattern
Flexible working, Full-time
Number of jobs available
1
Contents
- Location
- About the job
- Benefits
- Things you need to know
- Apply and further information
Location
Canary Wharf, London
About the job
Job summary
We are currently looking for an Associate Scientific Assessor to join our Benefit Risk Evaluation I Function within the Safety & Surveillance group.
This is a full-time opportunity, on a 12 month fixed term contract/internal move or temporary promotion basis. The role will be based in 10 South Colonnade, Canary Wharf London, E14 4PU. Please be aware that this role can only be worked in the UK and not overseas.
Government departments and agencies are working towards implementing a minimum 60% attendance in office sites.
We are currently implementing a flexible, hybrid way of working, with a minimum of 8 days per month working on site to enable the 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.
Who are we?
The Medicines and Healthcare products Regulatory Agency enhance and improve the health of millions of people every day through the effective regulation of medicines and medical devices, underpinned by science and research.
The Safety and Surveillance Group brings together into a single integrated structure devices and medicines safety expertise with enforcement capabilities. These functions will be supported by our data and evidence generating capabilities complementing our signal generating capabilities produced via the new Safety Connect System.
Job description
Medicines and devices have traditionally been regulated separately largely driven by different regulatory processes and ways of working. As science and technology drives increasing understanding of disease, it is also opening new opportunities for treatments; product profiles are changing, becoming ever more complex and the boundaries between disciplines are blurring. As such we have brought these functional capabilities together to better address the regulatory challenges of the future. Against this background and the drive to improve treatment availability for patients, safety remains at the heart of our decision making. As such the core objective of the Safety & Surveillance Group is to protect the public from risks associated with medicines and medical devices by:
- Ensuring a world class, comprehensive vigilance system that can promptly detect and monitor signals across the product life cycle
- Evaluating the benefit risk of medicines and devices for which signals or other safety concerns emerge and developing effective and measurable risk mitigation measures
- Ensuring patients and other stakeholders are involved in the regulatory processes and appropriate messages are issued for patients and stakeholders following regulatory decisions
- Deploying innovative interventions to reduce the criminal threat
- Exploiting data and embracing new technologies to develop the evidence to support our actions and understand their impact
What\βs the role?
To assist benefit risk evaluation assessors across the specialist therapeutic areas in the assessment of applications to amend the product information of medicines in relation to safety.
Safety and Surveillance: Benefit Risk Evaluation
Benefit Risk I
Benefit Risk II
Oncology, Haematology, Thrombotic disease
Musculoskeletal, Trauma and Cosmetic
Biosafety, Nonclinical and Emerging Technologies
Respiratory, Imaging and Critical Care
Vaccines, Infectious Diseases and Diagnostics
Cardiovascular and Fluid Management
Skin, Senses, Movement and Pain
Metabolic and Renal Systems
Psychiatric Disorders, Cognition and Mental Health
Gastrointestinal System, Nutrition, Endocrine and Fertility
Key responsibilities:
- Ensuring the quality and accuracy of Sentinel records.
- To assist BRE assessment teams with the processing of variation applications related to safety and applications to renew market authorisations
Person specification
Who are we looking for?
Our successful candidate will have:
- A degree in pharmacy, pharmacology, nursing, physiology, toxicology or other relevant life science discipline.
- Excellent IT skills and attention to detail combined with a desire to ensure that accurate product information is made publicly available.
- Experience of working in a regulatory environment or other relevant area and use of associated systems would be an advantage
- Ability to analyse and interpret data and make appropriate recommendations under pressure.
- Confidence and ability to work as part of a team in a fast paced environment.
- Excellent written and verbal communication skills
If you would like to find out more about this fantastic opportunity, please read our Job Description and Person Specification
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Benefits
Alongside your salary of Β£32,617, Medicines and Healthcare Products Regulatory Agency contributes Β£9,449 towards you being a member of the Civil Service Defined Benefit Pension scheme. Find out what benefits a Civil Service Pension provides.
- Annual Leave: 25 days annual leave on entry, rising by one day for each completed year of service to a maximum of 30 days and pro-rata for part-time staff. PLUS 8 bank holidays
- Privilege Leave: 1 day
- Hours of Work: 37 hours (net) per week for full time staff in all geographical locations, including London and pro rata for part-time staff
- Occupational Sick Pay (OSP): One month full pay/one month half pay on entry, rising by one month for each completed year of service to a maximum of five months full pay/five months half pay
- Mobility: Mobility clause in contracts allowing staff to be mobile across the Civil Service
- Civil Service Pension Scheme. Please see the link for further information For enquiries relating to the Civil Service Pension Schemes please contact MyCSP\βs Pension Service Centre directly on
- Flexible working to ensure staff maintain a healthy work-life balance
- Interest free season ticket loan or bike loan
- Employee Assistance Services and access to the Civil Service Benevolent Fund
- Eligibility to join the Civil Service Motoring Association (CSMA)
- Variety of staff and Civil Service clubs
- On-going learning and development
Things you need to know
Selection process details
The selection process:
We use the Civil Service Success Profiles to assess our candidates, find out more here.
- Online application form, including questions based on the Behaviour, Experience and Technical Success Profiles. Please ensure all application questions are completed in full; your application may not be considered if any responses are left blank. Our applications are CV blind, and our Hiring Managers will not be able to access your CV when reviewing your application.
- Interview, which can include questions based on the Behaviour, Experience, Technical and Strengths Success Profiles.
In the instance that we receive a high number of applications, we will hold an initial sift based on the lead criteria of: Experience of working in a regulatory environment or other relevant area and use of associated systems.
Applicants are assessed on whether they meet any mandatory requirements as well as the necessary skills and experience for the role. Applications are scored based on the competency-based answers provided- ensure you have read these thoroughly and allow sufficient time. You can view the competencies for this role in the job description.
Use of AI in Job Applications
Applicants must ensure that anything submitted is factually accurate and truthful. Plagiarism can include presenting the ideas and experience of others, or generated by artificial intelligence, as your own.
If you require any disability related adjustments at any point during the process, please contact as soon as possible.
Closing date: 16 September 2025
Shortlisting date: From 17 September 2025
Interview date: w/c 22 September 2025
Candidates will be contacted within a week of the sift and the interviews completed to inform them of the outcome.
If you need assistance applying for this role or have any other questions, please contact
Candidates will be subject to UK immigration requirements as well as Civil Service nationality rules. Further information on whether you are able to apply is available here.
Successful candidates must pass a disclosure and barring security check as well as animal rights and pro-life activism checks. People working with government assets must complete basic personnel security standard checks.
Certain roles within the MHRA will require post holders to have vaccinations, and in some circumstances, routine health surveillance. These roles include:
- Laboratory-based roles working directly with known pathogens
- Maintenance roles, particularly those required to work in laboratory settings
- Roles that involve visiting other establishments where vaccination is required
- Roles required to travel overseas where specific vaccination may be required.
Applicants who are successful at interview will be, as part of pre-employment screening subject to a check on the Internal Fraud Database (IFD). This check will provide information about employees who have been dismissed for fraud or dishonesty offences. This check also applies to employees who resign or otherwise leave before being dismissed for fraud or dishonesty had their employment continued. Any applicant\βs details held on the IFD will be refused employment. A candidate is not eligible to apply for a role within the Civil Service if the application is made within a 5 year period following a dismissal for carrying out internal fraud against government.
Any move to the MHRA from another employer will mean you can no longer access childcare vouchers. This includes moves between government departments. You may however be eligible for other government schemes, including Tax-Free Childcare. Determine your eligibility here.
Successful candidates may be subject to annual Occupational Health reviews dependent on role requirements. If you have any queries, please
In accordance with the Civil Service Commissioners\β Recruitment Principles our recruitment and selection processes are underpinned by the requirement of selection for appointment on the basis of merit by a fair and open competition. If you feel your application has not been treated in accordance with the Recruitment Principles and you wish to make a complaint, you should firstly contact Florentina Oyelami, Head of Talent Acquisition,
If you are not satisfied with the response you receive, you can contact the Civil Service Commission at:
Civil Service Commission
Room G/8
1 Horse Guards Road
London
SW1A 2HQ
Feedback will only be provided if you attend an interview or assessment.
Security
Successful candidates must undergo a criminal record check.
People working with government assets must complete baseline personnel security standard (opens in new window) checks.
Nationality requirements
This job is broadly open to the following groups:
- UK nationals
- nationals of the Republic of Ireland
- nationals of Commonwealth countries who have the right to work in the UK
- nationals of the EU, Switzerland, Norway, Iceland or Liechtenstein and family members of those nationalities with settled or pre-settled status under the European Union Settlement Scheme (EUSS)
- nationals of the EU, Switzerland, Norway, Iceland or Liechtenstein and family members of those nationalities who have made a valid application for settled or pre-settled status under the European Union Settlement Scheme (EUSS)
- individuals with limited leave to remain or indefinite leave to remain who were eligible to apply for EUSS on or before 31 December 2020
- Turkish nationals, and certain family members of Turkish nationals, who have accrued the right to work in the Civil Service
Further information on nationality requirements
Working for the Civil Service
The Civil Service Code sets out the standards of behaviour expected of civil servants.
We recruit by merit on the basis of fair and open competition, as outlined in the Civil Service Commission\βs recruitment principles .
The Civil Service embraces diversity and promotes equal opportunities. As such, we run a Disability Confident Scheme (DCS) for candidates with disabilities who meet the minimum selection criteria.
The Civil Service also offers a Redeployment Interview Scheme to civil servants who are at risk of redundancy, and who meet the minimum requirements for the advertised vacancy.
Diversity and Inclusion
The Civil Service is committed to attract, retain and invest in talent wherever it is found. To learn more please see the Civil Service People Plan and the Civil Service Diversity and Inclusion Strategy .
Apply and further information
Once this job has closed, the job advert will no longer be available. You may want to save a copy for your records.
Contact point for applicants
Job contact :
- Name : The Resourcing Team
- Email :
Recruitment team
- Email :
Further information
In accordance with the Civil Service Commissioners\β Recruitment Principles our recruitment and selection processes are underpinned by the requirement of selection for appointment on the basis of merit by a fair and open competition. If you feel your application has not been treated in accordance with the Recruitment Principles and you wish to make a complaint, you should contact the Resourcing Team at , in the first instance. If you are not satisfied with the response you receive you can contact the Civil Service Commission at: β β Civil Service Commission Room G/8 1 Horse Guards Road London SW1A 2HQ
Associate Scientific Assessor - 32,617 p.a. + benefits employer: Medicines and Healthcare Products Regulatory Agency
Contact Detail:
Medicines and Healthcare Products Regulatory Agency Recruiting Team
StudySmarter Expert Advice π€«
We think this is how you could land Associate Scientific Assessor - 32,617 p.a. + benefits
β¨Tip Number 1
Network like a pro! Reach out to people in the industry, attend events, and connect on LinkedIn. You never know who might have the inside scoop on job openings or can put in a good word for you.
β¨Tip Number 2
Prepare for interviews by researching the company and role thoroughly. Understand their mission and values, and think about how your skills align with what theyβre looking for. This will help you stand out during the interview.
β¨Tip Number 3
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β¨Tip Number 4
Donβt forget to apply through our website! Itβs the best way to ensure your application gets seen. Plus, we love seeing candidates who are proactive about their job search!
We think you need these skills to ace Associate Scientific Assessor - 32,617 p.a. + benefits
Some tips for your application π«‘
Read the Job Description Carefully: Before you start your application, take a good look at the job description. Itβs packed with info about what weβre looking for, so make sure you understand the key responsibilities and requirements. This will help you tailor your application to show us why youβre the perfect fit!
Be Specific in Your Answers: When filling out the application form, donβt just give generic answers. Use specific examples from your experience that demonstrate your skills and how they relate to the role. We want to see how youβve tackled challenges and achieved results in the past.
Check Your Spelling and Grammar: It might sound basic, but typos can really stand out. Take the time to proofread your application before hitting send. A well-written application shows us that you pay attention to detail, which is super important in our line of work.
Apply Through Our Website: Make sure you apply through our official website. Itβs the best way to ensure your application gets to us without any hiccups. Plus, youβll find all the info you need about the role and our company there!
How to prepare for a job interview at Medicines and Healthcare Products Regulatory Agency
β¨Know Your Stuff
Make sure you brush up on your knowledge of pharmacology, toxicology, and the regulatory environment. Familiarise yourself with the latest trends in safety and surveillance, as well as the specific therapeutic areas mentioned in the job description. This will show that you're not just interested in the role but also passionate about the field.
β¨Showcase Your Skills
Prepare to discuss your IT skills and attention to detail. Think of examples from your past experiences where you've successfully analysed data or worked under pressure. Be ready to explain how these skills will help you ensure the quality and accuracy of Sentinel records in this role.
β¨Team Player Vibes
Since the role involves working closely with assessment teams, be prepared to talk about your teamwork experiences. Share specific instances where you collaborated effectively, especially in fast-paced environments. Highlight your communication skills, as they are crucial for engaging with stakeholders.
β¨Ask Smart Questions
At the end of the interview, donβt forget to ask insightful questions about the Safety and Surveillance Group's current projects or challenges. This shows your genuine interest in the role and helps you understand how you can contribute to their mission of protecting public health.