| Location: | Remote |
|---|---|
| Salary: | £43,981 to £54,019 |
| Hours: | Full Time |
| Contract Type: | Fixed-Term/Contract |
| Placed On: | 14th August 2026 |
|---|---|
| Closes: | 4th September 2026 |
| Job Ref: | B02-11103 |
About the Role
Gynae-oncology Trials Group UK (GTG-UK) is a national clinical research group specialising in ovarian, endometrial, cervical and vulval cancer trials. Our goal is to improve gynaecological cancer outcomes for patients across the UK through:
The National Cancer Research Institute (NCRI) closed in June 2023, after over 20 years, leaving a huge gap in the co-ordination of cancer research across the UK. GTG-UK was formed to maintain the functions of the former NCRI Gynaecological Group, as per a national directive, and to continue formally representing the UK gynae-oncology community within international groups, such as, European Network of Gynaecological Oncology Trials (ENGOT) and the Gynaecologic Cancer Intergroup (GCIG). GTG-UK also collaborates widely with other clinical trials groups and charities in the UK. GTG-UK is a registered charity (charity number: 1216641), for further information www.gtguk.co.uk.
The post is funded for 2 years in the first instance
Applications should include a CV and a Cover Letter: In the Cover Letter, please provide evidence of the essential and desirable criteria in the Person Specification part of the Job Description. (By including a Cover Letter, you can leave blank the 'Why you have applied for this role' field in the application form, which is limited in the number of characters it will allow.)
We welcome applications from all candidates. Please note that applicants requiring Skilled Worker sponsorship should be aware that this role is not normally considered eligible for sponsorship under current UK immigration rules. Applicants who would require sponsorship to take up this role should be aware that UCL is therefore unlikely to be able to sponsor an appointment to this post.
About you
You will be a highly organised and proactive project management professional with experience supporting the delivery of clinical research studies or complex programmes within a regulated environment. You will have strong stakeholder management and communication skills, with the ability to build effective working relationships with investigators, sponsors, research teams and international collaborators.
You will be confident managing multiple priorities, coordinating competing workstreams and maintaining accurate documentation, while ensuring activities are delivered to agreed timelines and quality standards. With excellent attention to detail and problem-solving skills, you will be able to work independently, resolve routine operational issues and contribute to the continuous improvement of processes and ways of working.
You will be committed to collaborative working and motivated by the opportunity to support innovative clinical research that improves outcomes for women with gynaecological cancers across the UK and internationally.
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Customer advert reference: B02-11103
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