Freelance Research Nurse

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Syneos Health

WebsiteLinkedInAll Job Openings

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

• 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.

🎯 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 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.

🏖️ Benefits

• 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. • 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.