Part Time Research Nurse

Syneos Health

. Remain fully conversant with the trial protocol, Case Report Forms (CRFs/eCRF), off-site manual, supporting documents, procedures, timelines, and relevant SOPs .

Posted 9/23/2026part-timeRemote • SpainJuniorMid-LevelWebsite

Core Competencies

Role fit

Core Competencies

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

Highest-signal resume keywords

Registered NurseGCP CertificationClinical Trials ExperienceVenepunctureECG

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Nursing SkillsData DocumentationTrial ProceduresPatient RecruitmentAdverse Event Reporting

Soft Skills

Excellent Communication SkillsAbility to Work AutonomouslyTeam CollaborationTask Prioritization

Tools & Technologies

OutlookWordExcelPowerPoint

Certifications & Qualifications

GCP Certification

Industry Keywords

Clinical TrialsResearch DesignSOPsSubject ConfidentialityData Protection Compliance

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Remain fully conversant with the trial protocol, Case Report Forms (CRFs/eCRF), off-site manual, supporting documents, procedures, timelines, and relevant SOPs
Communicate with the Illingworth research nurse project manager, Research nurse manager, site staff, and Principal Investigator
Maintain accurate documentation and electronic data transfers while ensuring subject confidentiality, GCP, and data protection compliance
Attend Site Initiation Visits and other required meetings
Coordinate and complete subject trial visits on- and off-site with the RN team
Complete trial procedures and assessments according to protocol and SOPs and collect accurate data
Administer trial medication and facilitate its safe storage, transfer, and accountability
Process, package, and dispatch samples while liaising with courier companies and organizations
Assist with identifying eligible patients and patient recruitment into clinical trials
Provide patient information and support for on- and off-site care
Report adverse events, serious adverse events, and SUSARs to the site team and RNPM
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
Equivalent experience, skills, and/or education will also be considered

Benefits

Comp & perks

Part-time employment
Remote work (pre-approved)