Freelance Research Nurse

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

📋 Description

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

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

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

• Participate in Site Initiation Visits (SIV) as needed, along with any other essential meetings, such as multi-disciplinary, project management, and client-facing meetings.

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

• Ensure that all trial-related procedures and assessments are carried out in accordance with the protocol and relevant SOPs, while collecting data accurately.

• Administer trial medications per the protocol and oversee the secure storage, transfer, and accountability of trial medications in line with Illingworth SOPs.

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

• Aid in identifying potentially eligible patients for research projects and assist with patient recruitment into clinical trials, providing information and support for both on-site and off-site care.

• Ensure precise 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 actions.

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

⛳️ Requirements

• Must be a registered nurse with at least 2 years of post-qualification experience.

• Experience in research and clinical trials with GCP certification.

• Familiarity with research design and methodology is desirable.

• Experience and knowledge of clinical nursing skills such as Venepuncture and ECG is preferable.

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

• Excellent verbal and written communication skills.

• Strong ability to prioritize and manage multiple tasks effectively.

• Proficient in computer software, including Outlook, Word, Excel, and PowerPoint at a minimum.

🏝️ Benefits

• Tasks, duties, and responsibilities as outlined in this job description are not exhaustive.

• The Company retains the right to assign additional tasks, duties, and job responsibilities at its sole discretion and without prior notice.

• The Company is dedicated to adhering to the Americans with Disabilities Act, including providing reasonable accommodations when appropriate to help employees or applicants perform the essential functions of the job.