Research Assistant – Virtual Clinical Study

Sidekick

. Screen and enroll participants .

Posted 9/20/2026contractRemote • CanadaMid-LevelSenior💰 CA$30 per hourWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in human-subject research and participant management, with a strong focus on protocol compliance and data accuracy. Proficient in conducting virtual assessments and maintaining meticulous records in a clinical trial environment.

Highest-signal resume keywords

Human-Subject Research ExperienceGCP CertificationData Recording in Electronic SystemsVirtual Study Visit FacilitationHealth-Related Graduate Degree

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Data CaptureFunctional AssessmentsSymptom Diary MonitoringProtocol ComplianceParticipant Enrollment

Soft Skills

Attention to DetailCommunication SkillsFlexibility

Tools & Technologies

Electronic Data Capture SystemVideo Conferencing Tools

Certifications & Qualifications

GCP Certification

Industry Keywords

Clinical TrialsPhysiotherapyKinesiologyNursingPublic HealthRehabilitation Science

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Screen and enroll participants
Run virtual study visits by video
Guide participants through standardized functional assessments
Monitor daily symptom diaries and follow up on missed entries
Record data in the electronic data capture system according to protocol
Work alongside the study's physiotherapist investigator on assessment training
Work alongside a clinical trial consultant on protocol compliance

Requirements

What you’ll need

Graduate degree (or in progress) in a health-related field: physiotherapy, kinesiology, nursing, public health, rehabilitation science, or similar
Experience with human-subject research, ideally in a coordinator or RA role
Current GCP certification, or willingness to complete it before start
Comfortable running structured video sessions with participants and keeping meticulous records
Available 20–25 hours per week, with some flexibility for participant scheduling (evenings/weekends)
Based in Canada
Only applicants who have completed the application form will be considered

Benefits

Comp & perks

Fully remote, set your own hours within participant availability
Hands-on clinical trial experience from enrolment through study close, on a study intended for peer-reviewed publication
Training on standardized functional assessments from a practicing physiotherapist
Small team with direct access to the investigator and study sponsor