Contract Virtual Clinical Coordinator

IQVIA

. Conduct remote clinical activities in accordance with study protocols, SOPs, and GCP .

Posted 10/27/2026full-timeRemote • United StatesMid-LevelSenior💰 $33,000 - $82,600 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in conducting clinical activities in compliance with study protocols, SOPs, and GCP, while effectively managing participant interactions and data collection. Proficient in utilizing study-specific software applications and maintaining professionalism in all communications.

Highest-signal resume keywords

Clinical Trial CoordinationGood Clinical Practice (GCP)Standard Operating Procedures (SOPs)Patient Recruitment and EnrollmentData Management

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical ResearchData CollectionStudy Protocol ComplianceAdverse Event ReportingInformed Consent ManagementClinical Follow-Up ActivitiesStudy Equipment ManagementAttention to DetailVirtual CommunicationClinical Trial Documentation

Soft Skills

Verbal CommunicationWritten CommunicationProfessionalismParticipant SupportTeam Collaboration

Tools & Technologies

Study-Specific Software ApplicationsClinical Research Data Systems

Industry Keywords

Clinical TrialsLife SciencesHealthcareResearch Participant ManagementIRB Compliance

About the role

Key responsibilities & impact

Conduct remote clinical activities in accordance with study protocols, SOPs, and GCP
Identify, recruit, and virtually enroll eligible patients for clinical trials
Collect, maintain, and securely store clinical research data
Educate potential participants and manage informed consent through virtual interactions
Guide participants and provide reminders to support study compliance
Conduct clinical trial follow-up activities
Monitor participants, report adverse events promptly, and ensure compliance with IRB-approved protocols
Support the research participant call center
Maintain professionalism in participant interactions
Assist with study equipment management, tracking, functionality, and documentation
Communicate updates and provide support to MCRA clinical affairs staff and clients under senior staff guidance
Perform additional duties and projects as assigned

Requirements

What you’ll need

Bachelor’s degree required (preferably in a life sciences or healthcare-related field)
Minimum of three years of experience as a Clinical Coordinator or in a comparable clinical research role
Strong attention to detail
Excellent verbal and written communication skills
Working knowledge of study-specific software applications and equipment
Knowledge of Standard Operating Procedures (SOPs), Manual of Procedures, and Good Clinical Practice (GCP)
Ability to work weekday hours of 1:00 PM–9:00 PM PST
Ability to work Saturday and/or Sunday, 10:00 AM–6:00 PM PST

Benefits

Comp & perks

Potential incentive plans, bonuses, and/or other forms of compensation
Health and welfare and/or other benefits