Nurse

• Interpret and follow trial protocols, Case Report Forms, off-site manuals, supporting documents, procedures, timelines, and SOPs
• Communicate with the Illingworth research nurse project manager, research nurse manager, site staff, and Principal Investigator
• Maintain accurate trial documentation and electronic data transfers while protecting subject confidentiality and complying with GCP and data protection requirements
• Attend Site Initiation Visits and other multidisciplinary, project management, and client-facing meetings as required
• Coordinate and complete on-site and off-site subject trial visits and ensure procedures, assessments, and data collection comply with the protocol and SOPs
• Administer trial medication and facilitate its safe storage, transfer, and accountability
• Process, package, and dispatch samples while liaising with courier companies and organizations
• Identify potentially eligible patients and support recruitment into clinical trials
• Report adverse events, serious adverse events, and suspected unexpected serious adverse reactions, including required follow-up
• Report suspected misconduct or fraud to Illingworth and associated companies

Nurse jobs in France

Freelance Research Nurse