
Job Overview
Location
FRA-Remote
Job Type
Full-time
Category
Software Engineering
Date Posted
June 25, 2026
Full Job Description
đź“‹ Description
- • Fully conversant with clinical trial protocols, Case Report Forms (CRFs/eCRF), off-site manuals, supporting documents, procedures, and timelines to ensure daily trial operations in compliance with all relevant SOPs.
- • Communicate effectively with Illingworth Research Nurse Project Managers (RNPM), Research Nurse Managers, site staff, and Principal Investigators to maintain seamless information flow across trial activities.
- • Maintain accurate and confidential documentation throughout the trial, including electronic data entry, adhering strictly to GCP guidelines and data protection regulations.
- • Attend Site Initiation Visits (SIV) and other required meetings, including multidisciplinary, project management, and client-facing sessions as needed.
- • Coordinate and conduct subject trial visits both on-site and off-site, ensuring all protocol-specified procedures and assessments are completed accurately and in accordance with SOPs.
- • Administer trial medications as per the protocol, and manage the safe storage, transfer, and accountability of investigational products in alignment with Illingworth SOPs.
- • Process, package, and dispatch biological and clinical samples, coordinating with courier services and external organizations according to project-specific requirements and documentation.
- • Assist in identifying eligible patients for clinical trials and support patient recruitment by providing clear information and ongoing care guidance for on- and off-site participation.
- • Accurately report adverse events (AEs), serious adverse events (SAEs), and suspected unexpected serious adverse reactions (SUSARs) to the site team and RNPM, and provide follow-up support as required.
- • Report any suspected misconduct or fraud involving trial conduct to Illingworth and associated companies immediately.
- • Work autonomously with initiative in a multidisciplinary team environment while maintaining high standards of clinical and operational precision.
- • Utilize computer software including Outlook, Word, Excel, and PowerPoint for documentation, communication, and data management tasks.
- • Ensure all activities comply with GCP, data privacy laws, and Illingworth’s internal policies to safeguard patient confidentiality and trial integrity.
- • Support patient experience by delivering clinical research services directly in the patient’s home, contributing to improved trial participation and quality of life.
- • Adapt to evolving trial demands and additional responsibilities as assigned by the company, with flexibility to meet changing project needs.
🎯 Requirements
- • Registered nurse with a minimum of 2 years’ post-qualification experience
- • Research and clinical trials experience with GCP certification
- • Knowledge of clinical nursing skills such as venepuncture and ECG
- • Ability to work autonomously in a multidisciplinary team environment
- • Excellent verbal and written communication skills
- • Good working knowledge of Outlook, Word, Excel, and PowerPoint
🏖️ Benefits
- • Per diem freelance compensation structure
- • Flexible scheduling aligned with trial needs
- • Opportunity to work directly with patients in home-based clinical research settings
- • Engagement with a global organization operating in over 45 countries
Skills & Technologies
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About Syneos Health, Inc.
Syneos Health is a global biopharmaceutical services organization providing clinical and commercial solutions. It integrates clinical development, outsourced commercialization, consulting, and communications services to accelerate the delivery of therapies to market. The company supports pharmaceutical, biotechnology, and medical device clients across all phases of product development and commercialization, operating in North America, Europe, and Asia-Pacific.
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