JOB SUMMARY

The Research Assistant Practitioner will work as part of the clinical research team to support the safe conduct of research in accordance with the Research Governance Framework and Good Clinical Practice guidelines and provide assurance that the rights, safety and well-being of trial participants are protected.
The post-holder will work with the research team to provide technical, practical and clinical assistance for research projects. As a member of the Clinical Trials Team they will provide core support within this multidisciplinary setting. S/he will support the relevant study portfolio and deliver recruitment accrual in line with performance and monitoring objectives. If you are a motivated and enthusiastic person with an interest in research, we would welcome your application.
Informal visits or telephone enquiries are highly recommended.

ABOUT US

As an organisation, the NHS offers a wide range of benefits including flexible working, fantastic pension contributions, market leading annual leave allowance, career progression and regular conversations, not to mention our Blue Light Card and NHS exclusive discounts.
The benefits of working in Somerset include the idyllic countryside, with our areas of outstanding beauty and stunning coastlines. You will get to enjoy these perks whilst still only being a stone’s throw away from bustling city centres like Bristol, Bath and Exeter and only two hours away from London.
There are excellent educational facilities in the area and, when compared to other regions, house prices are reasonable. You will to experience the best of both in Somerset, the countryside and the cosmopolitan - there is truly something for everyone!

JOB DESCRIPTION

For more details and further information about the role, please see the attached job description and person specification.

We are seeking a motivated and dynamic practitioner to support our established acute research team. The post holder will be responsible for the implementation and monitoring of the clinical requirements associated with research to ensure optimum delivery of clinical trials. You will ensure that all research procedures are conducted according to study protocols and will be responsible for the recruitment, data collection and care of research participants with a focus on providing a quality experience. You will need excellent communication, organisational and time management skills. You will be expected to work in an autonomous, proactive and organised manner to deliver clinical research and produce robust quality data, within deadlines and to achieve NIHR targets.