BridgewaterSurgeries is a large teaching practice with a background in research. We have an exciting role to become a research nurse to support the practice to drive growth and expand our non-commercial research capabilities.
Main duties of the job
This permanent fulltime role has scope for growth and will suit a candidate who has experience and demonstrable interest in research. We will be looking for someone who has knowledge of Good Clinical Practice and can implement the principles of Good Clinical Practice. We are looking for a candidate with skills to conduct studies in a safe environment for our participants following protocols. You will be expected to take charge of clinics under the supervision of our GP Research Lead. As well as using your clinical skills you will be expected to collect data, liaise with research data teams to have this data entered in an accurate and timely manner and help answer queries raised by our or the research organisers team. You would also be expected to support the nursing team with routine nurse clinics dependent on research commitments.
About us
Our dynamic practice looks after 36,000 patients. We have 13 Partners, 12 salaried GPs and a very supportive team of Physician Associates, Pharmacists, Pharmacy Technicians, Practice Nurses, Nursing Associates, Health Care Assistants and Administrative staff. The post holder will be a key team player in a patient-facing role.
Job responsibilities
This research nurse role combines clinical expertise with the coordination and management of research studies. The candidate will act as a central point of contact between patients, investigators, and regulatory authorities, ensuring all research is delivered safely, ethically, and to the highest standards in alliance with Good Clinical Practice guidelines.
ClinicalResponsibilities
Assessing, screening, and recruiting suitable patients/participants for research studies
providing ongoing review of clinical trial participants and the delivery of clinical investigations and treatments, as defined by the clinical trial protocol.
Obtaining informed consent where appropriate, ensuring participants understand the study, risks, and rights.
Performing clinical procedures such as blood sampling, administering study medications, monitoring vital signs, and managing and recording side effects.
Manages the patient schedule to ensure all observations, interventions and procedures are carried out in accordance with the trial protocol
Acting as a patient advocate, ensuring safety and wellbeing throughout the study.
Ensuring compliance with ethical approvals, research governance, and legal requirements.
Upholding confidentiality and data protection standards.
Research & AdministrativeResponsibilities
Ensuring strict adherence to research protocols, Good Clinical Practice (GCP), and ethical standards.
Collecting, recording, and managing study data accurately and securely.
Coordinating study visits, follow-ups, and assessments.
Liaising with doctors, investigators, and multidisciplinary teams involved in the research.
Reporting adverse events or complications promptly within the expected time frame.
Data management, ensuring source data is recorded accurately and inputted into the electronic case report forms in a timely manner in accordance with the study protocol
Works autonomously to co-ordinate different aspects of trial procedures.
Responsible for ensuring all studies achieve recruitment targets and timelines.
Responsible for assessing and evaluating any potential cost implications associated with clinical trials. Liaising with the practice manager, and other Research staff during feasibility process.
Submitting Expressions of Interest to potential research sponsors.
Work within the Standard Operating Procedures for Research, Good Clinical Practice and relevant clinical trial protocols.
Education & Communication
Educating participants and their families about the research process.
Acting as a point of contact between patients, investigators, and external research bodies.
Informing staff or other healthcare professionals about study procedures.
Promoting awareness of clinical research within the healthcare setting.
Ensuring your own training records are compliant and remain up to date in accordance with GCP
Person Specification
Experience
* Clinical research, direct patient care
* dealing with a wide range of people, computer systems, including Microsoft Office, SystmOne clinical system, working in a GP practice,
* strong knowledge of anatomy
Qualifications
* GCSE grade A to C in English and Maths
Disclosure and Barring Service Check
This post is subject to the Rehabilitation of Offenders Act (Exceptions Order) 1975 and as such it will be necessary for a submission for Disclosure to be made to the Disclosure and Barring Service (formerly known as CRB) to check for any previous criminal convictions.
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