Freelance Research Nurse

Syneos Health

. Interpret and follow trial protocols, Case Report Forms, off-site manuals, supporting documents, procedures, timelines, and SOPs .

Posted 10/2/2026part-timeRemote • FranceJuniorMid-LevelWebsite

Core Competencies

Role fit

Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in clinical trial management, including adherence to protocols, GCP compliance, and effective communication within multidisciplinary teams. Proficient in clinical nursing skills and capable of managing trial documentation and patient recruitment.

Highest-signal resume keywords

Registered NurseGCP CertificationClinical Trials ExperienceVenepunctureECG

ATS Keywords

Tailor your resume

Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills

Clinical Nursing SkillsTrial Protocol InterpretationData Collection ComplianceAdverse Event ReportingPatient Recruitment

Soft Skills

Excellent Communication SkillsAbility to Work AutonomouslyTeam CollaborationTask Prioritization

Tools & Technologies

OutlookWordExcelPowerPoint

Certifications & Qualifications

GCP Certification

Industry Keywords

Clinical TrialsResearch DesignSOPsSubject ConfidentialityData Protection

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Interpret and follow trial protocols, Case Report Forms, off-site manuals, supporting documents, procedures, timelines, and SOPs
Communicate with the Illingworth research nurse project manager, research nurse manager, site staff, and Principal Investigator
Maintain accurate trial documentation and electronic data transfers while protecting subject confidentiality and complying with GCP and data protection requirements
Attend Site Initiation Visits and other multidisciplinary, project management, and client-facing meetings as required
Coordinate and complete on-site and off-site subject trial visits and ensure procedures, assessments, and data collection comply with the protocol and SOPs
Administer trial medication and facilitate its safe storage, transfer, and accountability
Process, package, and dispatch samples while liaising with courier companies and organizations
Identify potentially eligible patients and support recruitment into clinical trials
Report adverse events, serious adverse events, and suspected unexpected serious adverse reactions, including required follow-up
Report suspected misconduct or fraud to Illingworth and associated companies

Requirements

What you’ll need

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
Ability to work in Lille, France
Equivalent experience, skills, and/or education will also be considered

Benefits

Comp & perks

Part-time employment
Remote work (pre-approved)
Opportunity to be added to the talent pipeline and considered for future roles