Local Contractor - Research Nurse (per diem) - Lavaveix-Les-Mines area (France)

📋 Description

• • Serve as a per diem Research Nurse providing on- and off-site clinical research services to patients participating in clinical trials within the Lavaveix-les-Mines area, France.
• • Fully understand and adhere to the trial protocol, Case Report Forms (CRFs/eCRF), off-site manuals, supporting documents, procedures, timelines, and all relevant Standard Operating Procedures (SOPs).
• • Communicate effectively with the Illingworth Research Nurse Project Manager (RNPM), Research Nurse Manager, site staff, and Principal Investigator to ensure seamless information flow and trial coordination.
• • Maintain accurate, confidential, and compliant documentation throughout the trial, including electronic data entry in accordance with GCP and data protection regulations.
• • Attend Site Initiation Visits (SIV) and other required meetings, including multidisciplinary, project management, and client-facing sessions as needed.
• • Coordinate and conduct patient trial visits both on-site and off-site, ensuring all protocol-specified procedures and assessments are completed accurately and in compliance with SOPs.
• • Administer trial medications according to the protocol and ensure safe storage, transfer, and accountability of investigational products per Illingworth SOPs.
• • Process, package, and dispatch biological and clinical samples in alignment with project requirements, coordinating with courier services and external organizations.
• • Assist in identifying and recruiting eligible patients for clinical trials by providing information, support, and guidance for on- and off-site care.
• • Accurately report adverse events (AEs), serious adverse events (SAEs), and suspected unexpected serious adverse reactions (SUSARs) to the site team and RNPM, and support required follow-up actions.
• • Report any suspected misconduct or fraud to Illingworth and associated companies immediately.
• • Utilize computer software including Outlook, Word, Excel, and PowerPoint for daily documentation, communication, and data management tasks.
• • Work autonomously with initiative while collaborating within a multidisciplinary team environment to deliver high-quality patient-focused clinical research services.
• • Ensure compliance with all regulatory standards, including Good Clinical Practice (GCP), and maintain patient confidentiality at all times.
• • Adapt to evolving trial demands and perform additional duties as assigned by the Company, consistent with operational needs and regulatory obligations.