
Job requirements
Requirements from the employer’s person specification. These describe the role, not your personal match.
Essential
13 listedRequirements the employer expects applicants to meet.
- Other
Working in a mobile/agile way (A/I)
- Other
Commitment to equality, diversity and inclusion. (A/I)
- Experience
Experience working with individuals with mental health difficulties in a clinical or research setting (A/I)
- Experience
Experience of data management in secure clinical or research databases, ensuring high data quality and correct documentation and adherence to study protocols, including lone working (A/I)
- Experience
Experience of conducting PPI and public engagement activities (A/I)
- Qualifications
Degree qualification in relevant health sciences (e.g. nursing, psychology or sociology) (A)
- Qualifications
Completion of Good Clinical Practice training in the last 2 years or willingness to complete prior to commencing role (A)
- Knowledge and Skills
Excellent communication and interpersonal skills. (A/I)
- Knowledge and Skills
Highly motivated with the ability to work as part of a team and on an individual basis. (A/I)
- Knowledge and Skills
Knowledge of research methods and statistical procedures (A/I)
- Knowledge and Skills
Understands the research process and the application of research in improving healthcare. (A/I)
- Knowledge and Skills
Competence in standard PC packages (Word, Excel) (A/I)
- Knowledge and Skills
Demonstrates clear attention to detail and an organised approach to co-ordinating study activities and managing data (A/I).
Desirable
11 listedAdditional qualities the employer would prefer.
- Other
Occasional work outside of core hours to meet participants’ availability (A/I)
- Experience
Current or recent experience of working with people who have experienced trauma (A)
- Experience
Experience of conducting qualitative interviews (A)
- Experience
Experience in administering psychometric scales or willingness to train (A)
- Experience
Experience of recruiting participants to research studies including informed consent (A/I)
- Experience
Experience conducting research at a clinical interface or within a randomised controlled trial (A/I)
- Qualifications
A degree or diploma with a substantial research component (A)
- Qualifications
Higher degree/formal study of research design and methods in clinical or social settings (A)
- Knowledge and Skills
Commitment to obtain underpinning knowledge through work-based learning (A/I)
- Knowledge and Skills
Completing and scoring of research rating scales (A/I)
- Knowledge and Skills
Data management and analysis skills using software such as SPSS, NVivo (A/I)
Job overview
Imagine if the work you did today could impact on how mental health care is delivered tomorrow. An exciting opportunity has arisen join the Research and Development (R&D) Team at South London and Maudsley NHS Foundation Trust. A key aspect of this role is working on the delivery on a new randomised controlled trial.
This is an excellent development opportunity for a motivated and hardworking individual to gain experience in being part of a research team, expand their own knowledge of practice through supporting the delivery of research studies taking place within the trust. The portfolio of studies and locations offers the chance for this role to be both challenging and rewarding for the right candidate.
Main duties of the job
Key Responsibilities Include:
To work as part of the research growth and delivery team as a member of the DIAMONDS study, which is a randomised controlled trial.
To interact appropriately with research participants, service users, their carers and relatives, with the ability to convey the goals of the research in a friendly manner.
Participate in and contribute towards multi-disciplinary meetings within the unit, as well as liaising with health professionals outside of the research team as required.
To support the recruitment of participants to research studies in mental health through liaison with local research networks and clinical teams
To assist in obtaining valid informed consent to take part in research studies, providing complex verbal and written information in the process of explaining study involvement.
To collect research data through standardised assessment measures completed with participants.
To maintain Trust records and any trial databases and, ensuring entries are complete, accurate and up-to-date in accordance with the Trust policies, the protocol and Good Clinical Practice guidelines
Any other duties appropriate to the grade.
Detailed job description and main responsibilities
Communications and Working Relationships
- R&D departments, SLaM , SLP and KHP
- Matrons, Service General Managers, Service Delivery Managers
- Consultants and Junior Medical Staff
- Nursing Staff, Clinical Nurse Specialists
- Allied Health Professionals
- Administrative and Clerical Support Staff
- Lead Nurses/Co-ordinators, Research Delivery Managers and other research delivery staff
- South London CRN clinical divisions
- Professional and Technical staff
- Staff within non-commercial bodies and pharmaceutical companies and/or sponsors
Duties and Responsibilities
Clinical:
- Carry out planned care required by the clinical trials protocol for patients and volunteers without direct supervision
- Delivering on a RCT as a DIAMOND coach
- Responsible for screening and recruiting to clinical studies. This includes both randomised clinical trials and other high-quality clinical studies. The role will involve working closely with multidisciplinary clinical teams
- To support patients to make informed choices concerning their involvement in research.
- Ensure that written informed consent from a participant has always been obtained for any research taking place within the Trust.
- Maintain all data and case report forms relating to clinical trials in accordance with the regulatory and governance environment for NHS research.
- Report any deviation on research protocols to senior staff and implement agreed changes in care programme.
Management:
- Required to use own initiative, take responsibility for decision-making and prioritise own workload within a team and individual context.
- Work autonomously within the boundaries of own competencies and capabilities, seeking advice from Principal Investigator/ study team/R&D team as necessary.
- Support the coordination and organisation of study processes, including scheduling meetings, preparing documentation, and maintaining accurate records to ensure smooth delivery of the project.
- Support engagement of lived experience advisors across the project including research co-design workshops.
Administration:
- Maintain a safe environment in accordance with the Health and Safety at Work Act.
- Maintain accurate documentation in research documents and patient notes and comply with Trust and research governance policies and procedures.
- Communicate effectively at all times and maintain a harmonious working environment.
- Ensure the economical use of resources.
- Enter data accurately and promptly into service and study databases, ensuring these are auditable and complete.
- Good command of software packages such as Excel, word, MS Forms, SPSS, NVivo
Education and Training:
- Assist in the education and support of health care professionals to enable them to care for clinical trial patients and recruit to clinical trials where appropriate.
- Maintain an up-to-date knowledge of research related topics particularly related to clinical trials.
- Assess the needs of participants, relatives and carers and provide them with information as requested.
- Educate participants, family and those who volunteer for clinical trials before, during and after clinical studies and investigations.
- Assist the R&D Nurse Manager in orientating all new staff to the department.
Other:
- Understand and adhere to Trust policies and procedures.
- Maintain patient confidentiality and standards of Good Clinical Practice (GCP) at all times.
Applicant requirements
This post is subject to the Rehabilitation of Offenders Act 1974 (Exceptions) Order 1975 (Amendment) (England and Wales) Order 2020 and it will be necessary for a submission for Disclosure to be made to the Disclosure and Barring Service.
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Applying for this NHS job
This advert is for Research Assistant with South London and Maudsley NHS Foundation Trust in Beckenham, England. It is listed as a Band 5 Research assistant role. The advertised salary is £38,488 - £46,852 per annum inclusive of HCAS. The contract type is 12 months (Fixed term or Secondment). The application deadline is 28 Sep 2026.
Before you apply, compare the job description with the person specification and mirror the employer's essential criteria in your supporting information. Use the vacancy title, employer, location, salary, contract type, closing date and posted date (14 Sep 2026) to decide whether this role fits your current NHSjob search. If the employer can close applications early, prepare the application before the stated deadline rather than waiting for the final day.
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