Research Nurse – Local Contractor

🔥 0 minutes ago

🗣️🇫🇷 French Required

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Syneos Health

10,000+ employees

🧬 Biotechnology

💊 Pharmaceuticals

⚕️ Healthcare Insurance

Biotechnology • Pharmaceuticals • Healthcare Insurance

Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. They translate unique clinical, medical affairs, and commercial insights into outcomes to address modern market realities. By utilizing advanced technologies and insights, Syneos Health collaborates with clients to speed the delivery of important therapies to patients worldwide, offering services that span the entire clinical-to-commercial spectrum.

📋 Description

• Be fully conversant with the trial protocol, Case Report Forms (CRFs/eCRF), off-site manual (if applicable), supporting documents, procedures, and timelines to enable the 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 data transfer in accordance with Illingworth SOPs throughout the trial, ensuring subject confidentiality and compliance with GCP and data protection requirements. • Attend Site Initiation Visits (SIVs) as required and participate in other necessary meetings, including multidisciplinary, 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 per the protocol and ensure safe storage, transfer and accountability of trial medication in accordance with Illingworth SOPs. • Process, safely package and dispatch samples, liaising with courier companies and partner organisations 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 assistance for on- and off-site care. • Ensure accurate reporting of adverse events (AEs) and serious adverse events (SAEs)/suspected unexpected serious adverse reactions (SUSARs) to the site team and relevant RNPM, and provide support for any additional follow-up required. • Report any suspected misconduct or fraud to Illingworth and associated companies.

🎯 Requirements

• 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 is desirable. • Experience and competency in clinical nursing procedures such as venepuncture and ECG preferred. • Ability to work autonomously and use initiative while functioning effectively within a multidisciplinary team. • Excellent verbal and written communication skills. • Ability to prioritise and manage multiple tasks. • Good working knowledge of computer software including Outlook, Word, Excel and PowerPoint as a minimum.

🏖️ Benefits

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

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