Per Diem Freelance Research Nurse - Nice (France)

Syneos Health, Inc.; Montrouge; Sur place; EUR 40 000 - 50 000; Plein temps

Résumé du poste

A clinical research organization is seeking a Registered Nurse to support clinical trials in Montrouge, France. This role focuses on patient care coordination, facilitating communication with healthcare providers, and ensuring compliance with study protocols. Candidates should possess a minimum of 2 years of post-qualification nursing experience and GCP certification. The position requires excellent communication skills and the ability to work independently in a multidisciplinary environment. Join us in enhancing patient trial experiences and advancing clinical research.

Qualifications

• Registered nurse with a minimum of 2 years of post‑qualification experience.
• GCP certification and clinical trials experience required.
• Autonomous work ability in a multidisciplinary team.

Responsabilités

• Ensure smooth trial operations following protocols and SOPs.
• Coordinate patient care and assist in recruitment for trials.
• Document data accurately and maintain subject confidentiality.

Connaissances

Research and clinical trials experience

Excellent verbal and written communication skills

Clinical nursing skills

Ability to work autonomously

Prioritize and manage multiple tasks

Formation

Registered nurse with 2+ years of experience

GCP certification

Outils

Microsoft Office (Outlook, Word, Excel, PowerPoint)

Description du poste

Job Summary

Illingworth Research Group provides a range of patient‑focused clinical services to the pharmaceutical, healthcare, biotechnology and medical device industries, including mobile research nursing, patient concierge, medical photography and clinical research services. The organization operates in over 45 countries and brings clinical research directly into the homes of patients to improve trial experience and quality of life.

Location

Montrouge, 1, France

Responsibilities

• Fully conversant with the trial protocol, CRFs/eCRF, 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, research nurse manager, site staff and the Principal Investigator to ensure a smooth and efficient flow of information.
• Maintain accurate documentation and electronic data transfer as per Illingworth SOPs throughout the trial, ensuring subject confidentiality and adherence to GCP and data protection requirements.
• Attend Site Initiation Visits (SIV) and other necessary meetings, including multidisciplinary, project management and client‑facing meetings.
• Coordinate with the RN team to complete subject trial visits on‑ and off‑site, ensuring 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 support patient recruitment into clinical trials, providing information and support for 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 of 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

Illingworth Research Group is committed to equal employment opportunity and complies with applicable EEO and ADA requirements. The organization provides reasonable accommodations to employees and applicants with disabilities upon request.

Summary

Roles within the Research Nurse/Patient Concierge job family support patients participating in clinical research studies by coordinating care and facilitating communication with healthcare providers. The role helps patients understand study protocols, schedules appointments, addresses concerns and collaborates with research teams to monitor patient progress and collect data while ensuring compliance with regulatory standards. The position serves as a resource to help patients navigate the healthcare system and access necessary services throughout their research experience.