Description
We are seeking a Research Nurse to join our team on a per diem basis as an independent contractor. As a Research Nurse with Illingworth Research Group, you will play a crucial role in delivering high-quality clinical research services directly to patients in their homes.
Job Responsibilities
- Be fully conversant with the trial protocol, Case Report Forms (CRFs/eCRF), off-site manual, supporting documents, procedures, and timelines to enable the day-to-day running of the trial, including all relevant SOPs.
- Communicate effectively with the Illingworth research nurse project manager (RNPM), Research nurse manager, site staff, and the Principal Investigator to ensure a smooth and efficient flow of information.
- Maintain accurate documentation, including electronic transfer of data as per Illingworth SOPs throughout the trial, ensuring subject confidentiality, adhering to GCP and data protection requirements.
- Attend Site Initiation Visits (SIV) as required and any other necessary meetings, including multi-disciplinary, project management, and client-facing meetings.
- Coordinate and complete subject trial visits on- and off-site, working with the RN team to ensure all trial-related procedures and assessments are completed according to the protocol and relevant SOPs, and that data is collected accurately.
- Administer trial medication as per the protocol and facilitate the safe storage, transfer, and accountability of trial medication in accordance with Illingworth SOPs.
- Process and safely package and dispatch samples, liaising with courier companies and organizations in line with project requirements and supporting documents.
- Assist in identifying potentially eligible patients for research projects and assist with patient recruitment into clinical trials, providing information and support for those patients for on- and off-site care.
- Ensure the accurate reporting of adverse events (AEs) and serious adverse events (SAEs)/suspected unexpected serious adverse reactions (SUSARs) to the site team and relevant RNPM, providing support for any additional follow-up that may be required.
- Report any suspected misconduct or fraud to Illingworth and associated companies.
Qualifications
- Registered nurse with a minimum of 2 years' post-qualification experience.
- Research and clinical trials experience with GCP certification.
- Knowledge of research design and methodology desirable.
- Experience and knowledge of clinical nursing skills such as venepuncture and ECG preferable.
- Ability to work autonomously with initiative in a team within a multidisciplinary environment.
- Excellent verbal and written communication skills.
- Ability to prioritize and manage multiple tasks.
- Good working knowledge of computer software including Outlook, Word, Excel, and PowerPoint as a minimum.