Per Diem Freelance Research Nurse - Nice (France)

Syneos Health; Montpellier; Sur place; EUR 51 660 - 95 940; Temps partiel

Résumé du poste

Illingworth Research Group invites a Per Diem Freelance Research Nurse for assignments in Nice, France. The role supports clinical trials at patient sites, coordinating visits, data collection, and medication handling.

The ideal candidate is a qualified nurse with GCP training, strong communication skills, and the ability to work independently within a multidisciplinary team across trial sites. This freelance position offers day-to-day flexibility, exposure to diverse therapeutic areas, and a

Qualifications

• Registered nurse with at least 2 years post-qualification experience.
• GCP-certified for clinical trials.
• Knowledge of research design and methodology desirable.
• Venepuncture and ECG experience preferred.
• Ability to work autonomously within a multidisciplinary team.
• Excellent verbal and written communication skills.
• Strong task prioritization and multitasking ability.
• Proficient with Outlook, Word, Excel, and PowerPoint.

Responsabilités

• Fully conversant with trial protocol, CRFs/eCRF, off-site manual (if applicable), SOPs and timelines for day-to-day trial operations.
• Communicate effectively with the RN project manager, site staff and Principal Investigator to ensure smooth information flow.
• Maintain accurate documentation and data transfer per SOPs and data protection requirements.
• Attend Site Initiation Visits and other meetings as required.
• Coordinate and complete subject visits on- and off-site, ensuring data collection per protocol.
• Administer trial medication and manage storage/transfer per SOPs.
• Process and dispatch samples, liaising with courier services as required.
• Identify eligible patients and assist with recruitment for trials.
• Report adverse events and SUSARs to site team and RNPM.
• Report misconduct or fraud as needed.

Connaissances

Registered Nurse

GCP Certification

Clinical Research Design

Venepuncture/ECG

Autonomous Working

Verbal & Written Communication

Time Management

MS Office

Outils

Outlook

Word

Excel

PowerPoint

Description du poste

Per Diem Freelance Research Nurse - Nice (France)

Illingworth Research Group provides a range of patient focused clinical services to the pharmaceutical, healthcare, biotechnology and medical device industries. These include mobile research nursing, patient concierge, medical photography and clinical research services. Illingworth are experts with experience across all study phases and in a diverse range of therapeutic areas.

Illingworth Research Group is a global organization operating in over 45 countries, bringing clinical research directly into the home of the patient, to improve the experience of patients involved in clinical trials and the quality of their lives.

Job Responsibilities

• Fully conversant with the trial protocol, Case Report Forms (CRFs/eCRF), off‑site manual (if applicable), supporting documents, procedures, and timelines to enable day‑to‑day running of the trial including all relevant SOPs.
• Communicate effectively with the Illingworth research nurse project manager (RNPM), Research nurse manager, site staff and the Principal Investigator, to ensure a smooth and efficient flow of information.
• Maintain accurate documentation including electronic transfer of data as per Illingworth SOPs throughout the trial, ensuring subject confidentiality, adhering to GCP and data protection requirements.
• Attend Site Initiation Visits (SIV) as required and any other necessary meetings, including multi‑disciplinary, project management and client‑facing meetings.
• Coordinate (working with the RN team) and complete subject trial visits on‑ and off‑site. Ensure all trial related procedures and assessments are completed according to the protocol and relevant SOPs and that data is collected accurately.
• Administer trial medication as per the protocol, and facilitate the safe storage, transfer, and accountability of trial medication in accordance with Illingworth SOPs.
• Process and safely package and dispatch samples, liaising with courier companies and organizations in line with project requirements and supporting documents.
• Assist in identifying potentially eligible patients for research projects and assist with patient recruitment into clinical trials providing information and support for those patients for on‑ and off‑site care.
• Ensure the accurate reporting of adverse events (AEs) and serious adverse events (SAEs)/suspected unexpected serious adverse reactions (SUSARs) to the site team and relevant RNPM, providing support for any additional follow‑up that may be required.
• Report any suspected misconduct or fraud to Illingworth and associated companies.

Qualifications

• Registered nurse with a minimum of 2 years’ post qualification experience.
• Research and clinical trials experience with GCP certification.
• Knowledge of research design and methodology desirable.
• Experience and knowledge of clinical nursing skills such as Venepuncture and ECG preferable.
• Ability to work autonomously with initiative in a team within a multidisciplinary environment.
• Excellent verbal and written communication skills.
• Ability to prioritize and manage multiple tasks.
• Good working knowledge of computer software including Outlook, Word, Excel, and PowerPoint as a minimum.

Additional Information

Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.