Per Diem Freelance Research Nurse

This is a fully remote position, open to applicants in France.

📋 Description

• Fully knowledgeable about the trial protocol, Case Report Forms (CRFs/eCRF), off-site manual (if applicable), supporting documents, procedures, and timelines to facilitate the daily operations of the trial, including adherence to all relevant SOPs.

• Effectively communicate with the Illingworth research nurse project manager (RNPM), Research nurse manager, site personnel, and the Principal Investigator to ensure a seamless and efficient flow of information.

• Maintain precise documentation, including the electronic transfer of data in accordance with Illingworth SOPs throughout the trial, ensuring subject confidentiality while complying with GCP and data protection regulations.

• Attend Site Initiation Visits (SIV) as needed and participate in any necessary meetings, including multi-disciplinary, project management, and client-facing discussions.

• Coordinate with the RN team to complete subject trial visits both on-site and off-site.

• Ensure that all trial-related procedures and assessments are carried out according to the protocol and relevant SOPs, and that data is collected accurately.

• Administer trial medication following the protocol and ensure the safe storage, transfer, and accountability of trial medication in line with Illingworth SOPs.

• Process, safely package, and dispatch samples, coordinating with courier companies and organizations as per project requirements and supporting documents.

• Assist in identifying potentially eligible patients for research studies and aid in patient recruitment into clinical trials, providing information and support for on-site and off-site care.

• Ensure accurate reporting of adverse events (AEs) and serious adverse events (SAEs)/suspected unexpected serious adverse reactions (SUSARs) to the site team and relevant RNPM, offering support for any necessary follow-up.

• Report any suspected misconduct or fraud to Illingworth and its associated companies.

⛳️ Requirements

• Registered nurse with at least 2 years of post-qualification experience.

• Experience in research and clinical trials with GCP certification.

• Desirable knowledge of research design and methodology.

• Preferable experience and knowledge of clinical nursing skills such as Venepuncture and ECG.

• Ability to work independently with initiative in a multidisciplinary team environment.

• Excellent verbal and written communication abilities.

• Capability to prioritize and manage multiple tasks effectively.

• Proficient working knowledge of computer software including Outlook, Word, Excel, and PowerPoint as a minimum.

🏝️ Benefits

• N/A