| Location: | Oxford |
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| Salary: | £39,424 to £47,779 p.a |
| Hours: | Full Time |
| Contract Type: | Fixed-Term/Contract |
| Placed On: | 10th June 2026 |
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| Closes: | 7th July 2026 |
| Job Ref: | 186860 |
About the Role
You are invited to apply for the position of Project Manager to join Professor James Chalmers’ research team at the University of Oxford.
Professor James Chalmers specialises in translational and clinical research on respiratory diseases, including bronchiectasis, COPD and pneumonia, with a focus on microbiology, immunology, disease mechanisms and therapeutic strategies. You will be expected to provide high quality technical assistance to Prof. Chalmers and the other members of the research team.
The role involves coordinating EMBARC registry and research activities across European sites, including site set-up, supporting R&D and governance processes, and managing associated regulatory documentation and approvals. The postholder will oversee day-to-day registry operations, including site engagement, study performance and data query resolution, ensuring compliance with all relevant regulatory and governance frameworks. You will work with the group data analyst to ensure data analysis and request are delivered in a timely manner following approval from senior members of the group. You will contribute to the development and implementation of study procedures, support protocol amendments and assist with reporting, audits and monitoring activities.
You will coordinate study logistics, including shipment of supplies to sites and biological samples from sites as part of the EMBARC-BRIDGE biobanking study, alongside supporting biobank management and maintaining compliance standards. The role also includes liaising with industry partners, managing project budgets, supporting core trial management activities, and contributing to the development and costing of project proposals.
In addition, you will support the wider team with management, set-up and delivery of non-EMBARC research projects within the wider team, including managing all associated documentation and regulatory processes, and obtaining R&D approvals.
Acting as a central point of contact for participating centres, you will provide guidance, resolve queries, and facilitate effective communication across the network. You will work closely with clinical, academic, and operational teams, as well as external partners, to support research delivery, outputs, and the continued growth of the EMBARC programme.
This post is full-time and fixed term for 2 years
The post is only available as full-time on-site.
About You
To be considered for this position you should;
Benefits of working
Application Process
Applications for this vacancy are to be made online. You will be required to upload a supporting statement and CV 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. Click here for more information and advice on how to write an effective supporting statement.
Only applications received before 12:00 midday on 07/07/ 2026 will be considered. Interviews will be held as soon as possible thereafter.
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