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Syneos Health

Research Nurse

Syneos Health

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

Posted 9/30/2026part-timeRemote • AustraliaJuniorMid-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 trial protocols, GCP compliance, and effective patient recruitment. Proficient in clinical nursing skills and capable of maintaining accurate documentation and data integrity.

Highest-signal resume keywords
Registered NurseGCP CertificationClinical Trials ExperienceVenepunctureECG

ATS Keywords

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Applicant Tracking System Keywords

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

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 DesignSOPsPatient SupportData 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, 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 transfer while ensuring subject confidentiality, GCP, and data protection compliance
  • Attend Site Initiation Visits and other required meetings
  • Coordinate and complete on-site and off-site subject trial visits 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
  • Identify potentially eligible patients and assist with clinical trial recruitment and patient support
  • Report adverse events, serious adverse events, and suspected unexpected serious adverse reactions
  • Report suspected misconduct or fraud to Illingworth and associated companies
  • Join the talent pipeline for a possible upcoming opportunity rather than a live role

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 (Pre-Approved) work arrangement