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.

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