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Syneos Health

Research Nurse – Per Diem Independent Contractor

Syneos Health

. Maintain knowledge of trial protocols, Case Report Forms, off-site manuals, supporting documents, procedures, timelines, and SOPs .

Posted 10/22/2026part-timeRemote • CanadaJuniorMid-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 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

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

Hard Skills
Trial Protocol KnowledgeData Protection ComplianceTrial DocumentationPatient RecruitmentAdverse Event Reporting
Soft Skills
Excellent Communication SkillsAbility to Prioritize TasksTeam CollaborationAutonomous Work Initiative
Tools & Technologies
OutlookWordExcelPowerPoint
Certifications & Qualifications
GCP Certification
Industry Keywords
Clinical TrialsResearch DesignSOPsPatient CareMultidisciplinary Environment

Tech Stack

Tools & technologies
Google Cloud Platform

About the role

Key responsibilities & impact
  • Maintain knowledge of 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 ensuring confidentiality, GCP, and data protection compliance
  • Attend Site Initiation Visits and other multidisciplinary, project management, and client-facing meetings as required
  • Coordinate and complete on- 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
  • Assist with identifying eligible patients and recruiting patients into clinical trials
  • Provide information and support for patients receiving on- and off-site care
  • Report adverse events, serious adverse events, and suspected unexpected serious adverse reactions and support 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
  • Equivalent experience, skills, and/or education will also be considered

Benefits

Comp & perks
  • Per diem independent contractor arrangement
  • Part-time work
  • Remote work (pre-approved)