FAQs
What is the main responsibility of the Research and Development Data Administrator?
The main responsibility of the Research and Development Data Administrator is to perform data entry for a portfolio of clinical trials, ensuring high-quality data in line with the study protocol, Good Clinical Practice (GCP), and UK Medicines for Human Use Regulations.
Where will the post holder be based?
The post holder will be based across both Clinical Research Facility (CRF) sites at Bloomsbury and Queen Square according to the needs and requirements of the study portfolio.
What types of clinical trials will I be working on?
You will be working on a range of clinical trials, including first-into-human, complex, and innovative phase 3 trials, as well as experimental non-IMP studies.
Is there an opportunity for informal visits prior to applying?
Yes, candidates are encouraged to contact Melanie Dhanaratne, the Quality Assurance & Governance Manager, for further details or to arrange informal visits.
What is the commitment of UCLH regarding sustainability?
UCLH is committed to sustainability and has pledged to become a carbon net zero health service by setting an ambitious target of net zero for direct emissions by 2031 and indirect emissions by 2040.
When does the new NHS pay rate take effect?
The new NHS pay rate will take effect from autumn 2024. If your employment starts before the 2024/25 pay scales are implemented, you will be paid under the 2023/24 pay scales with any applicable backpay adjusted accordingly.
Who should I contact for further inquiries about the position?
For further inquiries about the position, you can contact Melanie Dhanaratne via email at melanie.dhanaratne@nhs.net.
What qualifications or experience are required for this role?
The job description does not provide specific qualifications or experience requirements; applicants are generally expected to be self-motivated and enthusiastic with relevant data administration skills.
Will the position require travel between sites?
Yes, the post holder will need to travel between the two CRF sites based on the dynamic requirements of the study portfolio.