
Per Diem Research Nurse – Adult
Posted 3 days ago

Posted 3 days ago
This is a fully remote position, open to applicants in United Kingdom.
• Oversee the daily operations of clinical trials in alignment with trial protocols, case report forms, supporting documents, procedures, timelines, and SOPs.
• Liaise with the Illingworth research nurse project manager, research nurse manager, site personnel, and Principal Investigator.
• Ensure the accuracy of trial documentation and electronic data transfers while upholding subject confidentiality, GCP, and data protection regulations.
• Participate in Site Initiation Visits and attend other multidisciplinary, project management, and client-facing meetings as necessary.
• Coordinate and conduct both on-site and off-site subject trial visits in collaboration with the RN team.
• Execute trial procedures and assessments as per protocols and SOPs while gathering precise data.
• Administer trial medications and ensure their secure storage, transfer, and accountability.
• Process, safely package, and send samples, coordinating with couriers and relevant organizations.
• Identify potentially eligible patients and assist with recruitment into clinical trials.
• Provide patient information and support for care both on-site and off-site.
• Report adverse events, serious adverse events, and SUSARs while supporting necessary follow-up actions.
• Report any suspected misconduct or fraud to Illingworth and its associated companies.
• Must be a registered nurse with at least 2 years of post-qualification experience.
• Experience in research and clinical trials with GCP certification is essential.
• Familiarity with research design and methodology is desirable.
• Preferably experienced in clinical nursing skills such as Venepuncture and ECG.
• Capable of working independently with initiative in a multidisciplinary team environment.
• Excellent verbal and written communication abilities.
• Proficient in prioritizing and managing multiple tasks effectively.
• Strong working knowledge of computer software, including Outlook, Word, Excel, and PowerPoint as a minimum requirement.
• Equivalent experience, skills, and/or education will also be taken into account.
• Part-time employment opportunities.
• Remote work arrangements (pre-approved).
• Professional engagement with multidisciplinary clinical research teams.
• Reasonable accommodations, when applicable, for employees or applicants with disabilities.
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