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

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Syneos Health

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10 000+ employés

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Healthcare • Consulting • Logistics

Syneos Health est une organisation de solutions biopharmaceutiques entièrement intégrée et leader, conçue pour accélérer le succès des clients. Ils transforment des intuitions cliniques, des affaires médicales et commerciales uniques en résultats pour répondre aux réalités du marché moderne. En utilisant des technologies avancées et des perspectives, Syneos Health collabore avec les clients pour accélérer la livraison de thérapies importantes aux patients dans le monde entier, offrant des services qui couvrent tout le spectre du clinique au commercial.

Description

• 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.

🎯 Exigences

• 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.

🏖️ Avantages

• Health insurance • 401(k) matching • Flexible work hours • Paid time off • Remote work options