Research Nurse - Per Diem

Syneos Health

. Become 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 • Washington • United StatesJuniorMid-Level💰 $50 - $60 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 trial protocols, GCP compliance, and accurate data collection. Proficient in patient recruitment, documentation, and 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

Trial Protocol KnowledgeData Protection ComplianceAdverse Event ReportingPatient RecruitmentMedication Administration

Soft Skills

Excellent Communication SkillsAbility to Prioritize TasksTeam CollaborationAutonomous Work Initiative

Tools & Technologies

OutlookWordExcelPowerPoint

Certifications & Qualifications

GCP Certification

Industry Keywords

Case Report FormsClinical Nursing SkillsResearch DesignSOP ComplianceSubject Confidentiality

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Become 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 electronically transfer data 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
Ensure trial procedures and assessments follow the protocol and relevant SOPs, with accurate data collection
Administer trial medication and facilitate 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
Accurately report adverse events, serious adverse events, and suspected unexpected serious adverse reactions
Report suspected misconduct or fraud and support additional follow-up as required

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

Benefits

Comp & perks

Company car or car allowance
Medical, dental, and vision health benefits
Company match 401(k)
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
Reasonable accommodations, when appropriate