Clinical Research Practitioner

Job summary

East Coast Community Health Care CIC is developing their Research and Development team. We are seeking a Clinical Research Practitioner to support the delivery of research in the community. This is a new role within ECCH. The successful candidate will become an integral part of the Quality team, with a focus on supporting the clinical teams to deliver research activity within the organisation and wider community.

This post would suit an individual with recent experience of clinical research in NHS/ Academic/ Pharmaceutical setting. This varied role would suit someone who has a flexible approach to working, is diligent, able to use their own initiative, likes working with other clinical teams and external partners and has an understanding of clinical research delivery and associated regulation.

There will be opportunities to promote research with clinical teams, patients and our wider community.

An interest in research and evidence based practice is essential.

There is flexibility in how the hours are worked across the working week. This post is offered between 30 and 37.5 hours per week. There will be no requirement to work Weekends or Bank Holidays.

Please note the job description is subject to agenda for change job matching.

Main duties of the jobThe post holder will be an integral part of the Quality team, focused on the delivery of research activity within the organisation. The post holder will be required to contribute to the development, assessment, and management of care pathways for participants in clinical trial activity, including recruitment, education and monitoring of trial participants as appropriate. The collection and documentation of accurate data.

The ability to manage a caseload of participants for data collection and follow up is essential.

The successful candidate will contribute to the identification of prospective research studies, be involved in the assessment of capacity and capability to deliver the study, study set up, data management and research delivery at sites across ECCH, so must be willing to travel as needed, and will be expected to work closely with research active clinicians.

Effective communication skills are crucial, as the post holder will be working with a broad professional and participant group. Engagement with colleagues, participants, and volunteers to promote research will be expected, with a focus on identifying barriers to research within the community. Collaboration with our research delivery partners, to seek new opportunities for research, develop and maintain working relationships.

The post holder will be working independently so must manage their own workload, possessing the necessary time management, organisational skills to work effectively and efficiently.

About us ECCH is well established health care provider and has been successfully delivering NHS care within the community since 2011. We provide a range of NHS, community health and social care services predominantly across the easterly region of the Norfolk/Suffolk borders.

We are aligned to NHS terms and conditions, and offer many employee benefits, to find out more about us visit our website -(Use the "Apply for this Job" box below). We are a social enterprise and staff owned organisation which means staff can opt to be shareholders and have a real say in how ECCH is run and evolves to deliver healthcare for the future.

At the heart of our ambition, we work in partnership with and for the community to become the provider and employer of choice for community healthcare.

Details Date posted
29 July 2026

Pay scheme

Agenda for change

BandBand 5

Salary
32,073 to 39,043 a year

Contract Permanent Working  pattern

Full-time

Reference number
849-OL-72

Job locations

Hamilton House Battery Green Road Lowestoft Suffolk NR
32 1DE
United Kingdom Job description

Job responsibilities
* To ensure that all study protocols, standard operating procedures, research governance, and good clinical practice guidelines are always adhered to.
* Ensure that all study documentation is maintained and stored confidentially.
* Support the study team in ensuring all reporting to regulatory bodies, and Research Networks (if applicable), is done in a timely manner.
* Support the study team to ensure that all research study equipment used is appropriately checked and calibrated (if applicable) with supporting documentation retained.
* Liaise with ICB Research and Development Team and sponsors if applicable to ensure all arrangements for research governance for each study are in place.
* Assist in the completion of participant assessments in accordance with study protocols, where appropriate within scope of practice and specified within study delegation log.
* Appropriately document and report all serious adverse events and incidents.
* Able to take informed consent in line with study protocols.
* To report and record serious adverse events according to regulatory and ECCH policies.
* Utilise computer skills for producing reports, spreadsheets and correspondence.
* Accurately…