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- Tasks: Manage clinical trials, ensuring timely data collection and compliance with regulations.
- Company: Join the NPEU CTU at the University of Oxford, a leader in perinatal research.
- Benefits: Enjoy hybrid working options and a supportive team environment.
- Why this job: Make a real impact in healthcare while developing your project management skills.
- Qualifications: Degree in biomedical sciences or relevant experience in clinical research required.
- Other info: Full-time role with part-time options available until October 2026.
The predicted salary is between 38674 - 46913 £ per year.
THIS POST COULD BE CONSIDERED AS A SECONDMENT OPPORTUNITY
The National Perinatal Epidemiology Unit, Clinical Trials Unit (NPEU CTU) are looking for an enthusiastic Trial Manager to join our team to provide project management for randomised controlled trials on the NPEU CTU portfolio. This is a great opportunity to join a friendly, supportive team with scope to contribute to wider development work of the Clinical Trials Unit.
The postholder will be based within the Nuffield Department of Population Health (NDPH) which contains world-renowned population health research groups and provides an excellent environment for multi-disciplinary research and teaching.
The NPEU is an internationally recognised, multi-disciplinary research unit based within the NDPH at the University of Oxford, Old Road Campus in Headington, Oxford. The unit undertakes research about pregnancy, childbirth and new-born babies.
As Trial Manager you will be the central administrative contact at the Coordinating Centre maintaining effective and efficient systems to ensure the trials are delivered according to milestones. You will co-ordinate the design, implementation and running of the clinical trials across participating hospital sites in the UK, ensuring timely data collection and Good Clinical Practice (GCP) compliance, and ensure they comply with NPEU CTU Standard Operating Procedures.
To be considered for this role you will have a degree in a biomedical or associated subject, or other relevant qualification or proven experience in clinical research. You will have line management experience, as well as an understanding of clinical research methodology, good clinical practice and knowledge of all UK regulations for clinical trials, GDPR and the research governance framework. Proven administrative, data and project management skills and excellent organisational skills and the ability to prioritise your workload are also essential for this position.
There will be opportunity for some hybrid office/remote working in line with department guidance.
The position is full time (part time up to 80% FTE considered) and fixed term until 31 0ctober 2026. The closing date for applications is noon on 5 September 2025.
For informal queries about the position, please contact Kayleigh Stanbury (kayleigh.stanbury@npeu.ox.ac.uk).
You will be required to upload a CV and Supporting Statement as part of your online application. The Supporting Statement should include a cover letter and should also clearly describe how you meet each of the selection criteria listed in the job description.
Committed to equality and valuing diversity.
Contact Person :
NDPH Recruitment Team
Vacancy ID :
181368
Contact Phone :
01865617933
Closing Date & Time :
05-Sep-2025 12:00
Pay Scale :
STANDARD GRADE 7
Contact Email :
recruit@ndph.ox.ac.uk
Salary (£) :
38674 – 46913
Trial Manager employer: University of Oxford
Contact Detail:
University of Oxford Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Trial Manager
✨Tip Number 1
Familiarise yourself with the specific clinical trials and research areas that the NPEU CTU focuses on. Understanding their portfolio will not only help you in interviews but also demonstrate your genuine interest in their work.
✨Tip Number 2
Network with current or former employees of the NPEU CTU. Engaging with them can provide valuable insights into the team culture and expectations, which can be beneficial during your application process.
✨Tip Number 3
Brush up on your knowledge of Good Clinical Practice (GCP) and UK regulations for clinical trials. Being well-versed in these areas will not only boost your confidence but also show that you are prepared for the responsibilities of the role.
✨Tip Number 4
Prepare to discuss your project management experience in detail. Think of specific examples where you've successfully managed projects, particularly in clinical research, as this will be a key focus during interviews.
We think you need these skills to ace Trial Manager
Some tips for your application 🫡
Understand the Role: Read the job description thoroughly to understand the responsibilities and requirements of the Trial Manager position. Make notes on how your skills and experiences align with what they are looking for.
Craft Your Supporting Statement: Your Supporting Statement should include a cover letter and clearly address each selection criterion mentioned in the job description. Use specific examples from your experience to demonstrate how you meet these criteria.
Tailor Your CV: Ensure your CV is tailored to highlight relevant experience in clinical research, project management, and any line management roles you've held. Focus on achievements that showcase your organisational skills and understanding of clinical trials.
Proofread and Submit: Before submitting your application, proofread all documents for spelling and grammatical errors. Ensure that your CV and Supporting Statement are formatted correctly and that all required documents are uploaded.
How to prepare for a job interview at University of Oxford
✨Know Your Trials
Familiarise yourself with the specific trials that the NPEU CTU is involved in. Understanding their methodologies and objectives will show your genuine interest and help you answer questions more effectively.
✨Highlight Relevant Experience
Be prepared to discuss your previous experience in clinical research and project management. Use specific examples to demonstrate how your skills align with the requirements of the Trial Manager role.
✨Understand GCP and Regulations
Brush up on Good Clinical Practice (GCP) guidelines and UK regulations for clinical trials. Being able to discuss these topics confidently will showcase your knowledge and suitability for the position.
✨Prepare Your Supporting Statement
Your Supporting Statement should clearly address each selection criterion listed in the job description. Tailor it to reflect how your qualifications and experiences make you the ideal candidate for the role.
