
10,000+ employees
đ„ Healthcare
đŒ Consulting
đŠ Logistics
Healthcare âą Consulting âą Logistics
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.
đ„ 17 hours ago
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10,000+ employees
đ„ Healthcare
đŒ Consulting
đŠ Logistics
Healthcare âą Consulting âą Logistics
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.
âą Interpret and follow trial protocols, Case Report Forms, off-site manuals, supporting documents, procedures, timelines, and SOPs âą Communicate with the Illingworth research nurse project manager, research nurse manager, site staff, and Principal Investigator âą Maintain accurate trial documentation and electronic data transfers while protecting subject confidentiality and complying with GCP and data protection requirements âą Attend Site Initiation Visits and other multidisciplinary, project management, and client-facing meetings as required âą Coordinate and complete on-site and off-site subject trial visits and ensure procedures, assessments, and data collection comply with the protocol and SOPs âą Administer trial medication and facilitate its safe storage, transfer, and accountability âą Process, package, and dispatch samples while liaising with courier companies and organizations âą Identify potentially eligible patients and support recruitment into clinical trials âą Report adverse events, serious adverse events, and suspected unexpected serious adverse reactions, including required follow-up âą Report suspected misconduct or fraud to Illingworth and associated companies
âą Registered nurse with a minimum of 2 years' post qualification experience âą Research and clinical trials experience with GCP certification âą Knowledge of research design and methodology desirable âą Experience and knowledge of clinical nursing skills such as Venepuncture and ECG preferable âą Ability to work autonomously with initiative in a team within a multidisciplinary environment âą Excellent verbal and written communication skills âą Ability to prioritize and manage multiple tasks âą Good working knowledge of computer software including Outlook, Word, Excel, and PowerPoint as a minimum âą Ability to work in Lille, France âą Equivalent experience, skills, and/or education will also be considered
âą Part-time employment âą Remote work (pre-approved) âą Opportunity to be added to the talent pipeline and considered for future roles
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