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Clinical Research Nurse
4 weeks ago
The successful candidate will work autonomously to assist in the management of research studies, maintaining effective communication with patients, carers, and professionals to ensure high-quality research delivery.
Key Duties- Manage and oversee a portfolio of research studies at various stages of completion and intervention.
- Carry out physical assessments, taking blood/urine samples and processing according to research study protocol.
- Care for research participants within the relevant sphere of practice and use opportunities to provide health promotion and patient education.
- Maintain accurate documentation of patient events in nursing/medical notes and Case Report Forms.
- Ensure that research specific investigations are undertaken as required by the protocol and obtain results in order to establish eligibility and safety to enter the research study.
- Safely administer any treatments/drugs that are given within the context of a clinical research trial.
- Assess and manage any adverse reactions occurring due to ongoing treatment of a participant in a study seeking advice from medical staff as appropriate and when required.
- Act as a resource for other research nurses/HCAs/admin staff within the research team.
- Be responsible for the delivery of allocated research studies.
- Ensure that the delivery of studies meet requirements with regards to the UK policy framework for health and social care research and the EU Clinical Trials Directive by implementing quality systems.
- Participate in Good Clinical Practice (GCP) training, keeping up to date with any changes in legislation or practice.
- Contribute to study set up, recruitment planning and study delivery.
- Be responsible for promoting the appropriate referral and recruitment of patients to clinical research studies.
- Ensure clear, accurate and concise records are kept for research projects in accordance with all regulatory requirements including the Data Protection Act.
- Ensure that data is transcribed accurately where required and assist with the maintenance of the Study Site File.
- Respond to data queries generated by the study coordinating team within a timely manner.
- Ensure the recording & reporting of adverse and serious adverse events that occur whilst the participant is in the research study.
- Assess and evaluate the progress of ongoing studies, maintaining accurate records of the status of studies and providing regular updates to the research team.
- Discuss ongoing study performance issues with the PI.
- Co-operate with external and internal audit, data monitoring and quality assurance.
- Advocate for research provide education and training on research projects to interested parties as required.
- Mentor new research nurses and provide clinical support as needed.
- Work on her/his own initiative, demonstrate a flexible approach to work and to function well as part of the wider Brownlow Team.
The ideal candidate will possess the following qualifications and experience:
- Registered Part 1 NMC.
- Qualification or experience in Research.
The successful candidate will have:
- Knowledge of clinical governance, confidentiality, data protection and information governance in primary care.
- Knowledge of the local and national health policy and wider health economy.
- Knowledge of safeguarding children and adults' policies and procedures.
- Experience of working within primary care.
- Minimum of 2 years band 6 experience.
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.
£35,392 to £50,056 a year Band 6/7 depending on experience.
