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Research Midwife
15 hours per week (Monday to Friday: 09:00 - 17:00 - Negotiable)
Fixed Term 12 Months Contract / Secondment Opportunity / Development Opportunity
Salary: £38,682. Max grade value is £46,580 per annum pro rata (dependant on experience)
Closing Date: 3rd November 2025
Interview Date: TBC
**This post may close early due to high numbers of applications, so you are advised to apply promptly.**
All correspondence for this vacancy will be sent by email; please check your account regularly including your Junk and SPAM areas.
A great and friendly place to work, so bring your passion, commitment and expertise and enjoy the opportunities to make a difference every day.
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The post holder will significantly contribute to the recruitment of Women & Children Research at George Eliot Hospital. They will facilitate the set-up, coordination and management of clinical research studies in a broad range of studies across several different departments. You will support the development a mixed research portfolio.
The post holder will contribute to high-quality clinical research by undertaking duties including recruitment and consenting of participants. They will facilitate care of patients in trials, including monitoring, observation, and supporting trial-related procedures.
They will maintain accurate records of data from research studies, ensuring integrity and protocol compliance. Although the role has a maternity focus, it will also support research across the broader Women & Children division, contributing to study development and delivery.
The post holder will ensure research safeguards participant wellbeing and complies with the UK Policy Framework for Health and Social Care Research (HRA, 2018), Good Clinical Practice (GCP), the Medicines for Human Use (Clinical Trials) Regulations (2004), and other relevant guidance.
Key Responsibilities
The Research Midwife supports the safe and effective delivery of clinical research, primarily in maternity but also across the Women & Children division. Working under the supervision of senior research staff, the post holder will recruit and consent participants, deliver care in line with study protocols, and maintain accurate documentation.
Responsibilities include monitoring patients, performing clinical procedures (e.g. venepuncture), and managing biological samples. The role supports both interventional and non-interventional studies, contributing to study setup, feasibility, and regulatory compliance. The post holder will ensure research is conducted in accordance with Good Clinical Practice (GCP), Trust policies, and relevant legislation.
You will liaise with multidisciplinary teams, attend study visits, and use IT systems to track progress. The role also involves promoting research awareness, supporting colleagues, and maintaining professional development in line with NMC requirements. Flexibility in working hours and travel may be required.
For a full comprehensive list of main responsibilities and duties, please kindly refer to job description and person specification attached.