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Syneos Health

Research Nurse – Per Diem

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 10/5/2026part-timeRemote • Hawaii • United StatesJuniorMid-Level💰 $45 - $55 per hourWebsite

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 NurseClinical Trials ExperienceGCP CertificationVenepunctureECG

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 Prioritize TasksTeam CollaborationAutonomous Work Initiative
Tools & Technologies
OutlookWordExcelPowerPoint
Certifications & Qualifications
GCP Certification
Industry Keywords
Case Report FormsSOPsResearch DesignData Protection ComplianceSubject Confidentiality

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 transfer 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, safely 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
  • 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 preferred
  • 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

Benefits

Comp & perks
  • Company car or car allowance
  • Medical, Dental and Vision health benefits
  • Company match 401k
  • Eligibility to participate in Employee Stock Purchase Plan
  • Eligibility to earn commissions/bonus based on company and individual performance
  • Flexible paid time off (PTO)
  • Sick time