Application Handler in London

Application Handler in London

London Full-Time 30000 - 40000 € / year (est.) Home office (partial)
Medicines and Healthcare Products Regulatory Agency

At a Glance

  • Tasks: Handle applications for clinical trials and investigations, ensuring smooth processing and communication.
  • Company: Join the Medicines and Healthcare products Regulatory Agency, making a difference in public health.
  • Benefits: Enjoy a competitive salary, flexible working, and opportunities for professional growth.
  • Other info: Dynamic work environment with a focus on collaboration and career development.
  • Why this job: Be part of a team that impacts millions through innovative healthcare solutions.
  • Qualifications: Ideal for graduates in Life Sciences or those with relevant experience in the medical sector.

The predicted salary is between 30000 - 40000 € per year.

We are currently looking for an Application Handler to join our Clinical Investigations & Trials Function within the Innovation & Compliance group. This is a full-time opportunity, on a permanent basis. The role will be based in 10 South Colonnade, Canary Wharf London, E14 4PU. 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. Please discuss this with the recruiting manager before accepting an appointment.

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 Innovation and Compliance Group delivers public health impact, world-leading research innovation, and a unique proposition via an ambitious Science Strategy which will balance innovation against sustainability and affordability. It is divided into four sub-Groups: Innovation Accelerator and Regulatory Science, Clinical Investigations and Trials, Standards and Compliance, and Innovative Devices.

The Clinical Investigations and Trials function ensure the efficient, pragmatic, proportionate and patient-centred advice for, and assessment of, Clinical Investigations into the performance and safety of medical devices and diagnostics as well as Clinical Trials of investigational medicinal products.

What’s the role? This is a support role that specialises in the handling of applications to the Unit for Clinical Investigations and Trials. Reporting to the Business Manager, the Application Handler acts as the dedicated point of contact for all technical and complex procedural queries referred from the other units and Groups across the Agency. The role is also responsible for overseeing allocation of applications and assisting with workload management, specifically with the monitoring of assessment targets and work queue management in the case management systems and maintaining good working relations with other Agency application processing staff.

Key responsibilities:

  • Process Clinical Trial and Clinical Investigation applications via appropriate case management systems and ensure allocation to appropriate assessors and reviewers.
  • Assist the Business Manager with workload management for the team.
  • Monitor assessment activities against targets within the Assessment team to identify peaks and troughs of workload on an individual and team basis.
  • Provide clear, concise, and timely communications with applicants and expert assessors as required, including the arranging and facilitation of external facing advice meetings between the internal and external stakeholders.
  • Assist in generating monthly and ad hoc metrics and reports for Unit and Group reports as well as longer term reports on Unit performance.
  • Generate metrics and reports as requested to respond to enquiries or questions, for example queries from ministers and FOI requests.
  • Assist with IT development projects and piloting new processes related to Clinical Trials and Clinical Investigations, as required.
  • Establish close links to application processing colleagues and ensure application tracking spreadsheets and databases are maintained, that applications are processed through the case management systems and output letters are generated appropriately.
  • Ensure Clinical Trial and Clinical Investigation applications have full end-to-end flow from applicant to assessor and back to the applicant with transparent tracking and communication.
  • Provide support for strategy and policy within the Unit for Clinical Investigations and Trials, particularly for application processing elements, technical aspects of applications, enquiry handling and advice meetings.

Person Specification:

Method of assessment: A=Application, T=Test, I=Interview, P=Presentation

Behaviour Criteria:

  • Making Effective Decisions (A, I)
  • Managing a Quality Service (A)
  • Delivering at Pace (A, I)
  • Communicating and Influencing (A, I)

Experience Criteria:

  • Proven experience of working in and managing a busy team demonstrating effective management, organisation and delegation skills (A, I)
  • Experience of working in the pharmaceutical, medical sector and/or regulatory sectors desirable (A)

Technical Criteria:

  • Graduate with Life Science or other relevant degree, or appropriate work experience in the pharmaceutical, medical sector and/or regulatory sectors or equivalent experience (A)
  • Excellent IT skills with proven ability to use and analyse data (A)

If you would like to find out more about this fantastic opportunity, please read our Job Description and Person Specification!

Please note: The job description may not open in some internet browsers. Please use Chrome or Microsoft Edge. If you have any issue viewing the job description, please contact careers@mhra.gov.uk.

The selection process:

We use the Civil Service Success Profiles to assess our candidates. Online application form, including a statement of suitability, of no more than 750 words demonstrating how you meet the person specification. 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. Please ensure not to include any personal identifying information on your supporting information. 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 Excellent IT skills with proven ability to use and analyse data and Demonstrates strong planning and organisational skills with proven ability to effectively manage changing priorities. 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 statement of suitability provided. You can view the criteria for this role in the job description.

Use of AI in Job Applications: Artificial Intelligence can be a useful tool to support your application, however, all examples and statements provided must be truthful, factually accurate and taken directly from your own experience. Where plagiarism has been identified (presenting the ideas and experiences of others, or generated by artificial intelligence, as your own) applications may be withdrawn and internal candidates may be subject to disciplinary action. Please see our candidate guidance for more information on appropriate and inappropriate use.

If you require any disability related adjustments at any point during the process, please contact careers@mhra.gov.uk as soon as possible.

Closing date: 31st May 2026

Shortlisting date: from 5th June 2026

Interview date: from 15th June 2026

If you need assistance applying for this role or have any other questions, please contact careers@mhra.gov.uk. 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’s 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.

Individuals appointed on level transfer will retain their existing salary and are responsible for ensuring they fully understand the financial implications of any potential move and the impact (if any) on their terms. If an individual is in any doubt, they should seek clarification before accepting a job offer.

Staff joining on promotion will receive up to a 10% increase of their current basic salary, or the pay band minimum, whichever is the greater. The individual will not retain any allowances paid by the former department/Agency, unless there are special circumstances, such as a reserved right to those allowances on transfer.

Successful candidates may be subject to annual Occupational Health reviews dependent on role requirements. If you have any queries, please contact careers@mhra.gov.uk.

In accordance with the Civil Service Commissioners’ 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, in the first instance, you should contact the MHRA Recruitment Team at careers@mhra.gov.uk. If you are not satisfied with the response you receive, you can contact the Civil Service Commission at: civilservicecommission.independent.gov.uk info@csc.gov.uk Civil Service Commission Room G/8 1 Horse Guards Road London SW1A 2HQ

Application Handler in London employer: Medicines and Healthcare Products Regulatory Agency

The Medicines and Healthcare products Regulatory Agency (MHRA) is an exceptional employer, offering a dynamic work environment in the heart of Canary Wharf, London. With a strong commitment to public health and innovation, employees benefit from a flexible hybrid working model, opportunities for professional growth, and a collaborative culture that values contributions to vital healthcare advancements. Join us to be part of a team that makes a meaningful impact on millions of lives every day.

Medicines and Healthcare Products Regulatory Agency

Contact Detail:

Medicines and Healthcare Products Regulatory Agency Recruiting Team

StudySmarter Expert Advice🤫

We think this is how you could land Application Handler in London

Tip Number 1

Get to know the company! Research the Medicines and Healthcare products Regulatory Agency and their mission. Understanding their goals will help you tailor your conversations and show that you're genuinely interested in being part of their team.

Tip Number 2

Network like a pro! Connect with current employees on LinkedIn or attend industry events. Building relationships can give you insider info about the role and might even lead to a referral, which is always a bonus!

Tip Number 3

Prepare for the interview by practising common questions related to application handling and clinical trials. Use the STAR method (Situation, Task, Action, Result) to structure your answers and highlight your relevant experience.

Tip Number 4

Don’t forget to follow up after your interview! A quick thank-you email can leave a lasting impression and shows your enthusiasm for the position. Plus, it’s a great way to reiterate why you’re the perfect fit for the role.

We think you need these skills to ace Application Handler in London

Application Handling
Case Management Systems
Workload Management
Data Analysis
Communication Skills
Report Generation
Stakeholder Engagement

Some tips for your application 🫡

Read the Job Description Carefully:Before you start your application, take a good look at the job description. It’s packed with info on what we’re looking for, so make sure you understand the key responsibilities and person specification. This will help you tailor your application to show us why you're the perfect fit!

Craft a Strong Statement of Suitability:Your statement of suitability is your chance to shine! Keep it under 750 words and clearly demonstrate how your skills and experiences match our requirements. Use specific examples to back up your claims – we love seeing real-life applications of your abilities.

Be Clear and Concise:When filling out your application, clarity is key. Avoid jargon and keep your language straightforward. We want to understand your points easily, so make sure your writing is clear and to the point. Remember, less is often more!

Apply Through Our Website:Don’t forget to submit your application through our website! It’s the best way to ensure it gets to us without any hiccups. Plus, you’ll find all the necessary details and resources there to help you along the way. Happy applying!

How to prepare for a job interview at Medicines and Healthcare Products Regulatory Agency

Know Your Stuff

Make sure you understand the role of an Application Handler and the key responsibilities involved. Familiarise yourself with clinical investigations, trials, and the regulatory landscape. This will help you answer questions confidently and show that you're genuinely interested in the position.

Showcase Your IT Skills

Since excellent IT skills are a must for this role, be prepared to discuss your experience with case management systems and data analysis. Bring examples of how you've used technology to improve processes or manage workloads effectively in previous roles.

Communicate Clearly

As the role involves liaising with various stakeholders, practice articulating your thoughts clearly and concisely. You might be asked to explain complex procedures or provide advice, so demonstrating strong communication skills will be crucial.

Prepare for Behavioural Questions

Expect questions based on the Civil Service Success Profiles, particularly around making effective decisions and managing a quality service. Use the STAR method (Situation, Task, Action, Result) to structure your answers and highlight your relevant experiences.