Job Overview
Location
Durham, North Carolina, United States of America
Job Type
Full-time
Category
Operations
Date Posted
May 2, 2026
Full Job Description
đź“‹ Description
- • The Remote Visit Coordinator, US Regional Specialist is a key liaison between clinical teams, remote research clinicians, and investigator sites, ensuring the successful execution of remote and decentralized trial visits by supporting operational, technical, and administrative functions across assigned studies.
- • Day-to-day responsibilities include conducting outreach and training for investigator sites, onboarding research clinicians, managing system access (Study Hub, Thinking Cap), processing Visit Request Forms, assigning clinicians, coordinating visit logistics (supplies, equipment, courier), maintaining Smartsheet trackers, performing quality checks on documentation, delivering study-specific training, ensuring compliance with GCP, ICH, HIPAA, and IQVIA SOPs, serving as the primary liaison between sites and internal teams, providing ongoing support and retraining, and escalating issues to the RRC Lead for resolution.
- • IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence, dedicated to accelerating medical treatment development and improving patient outcomes worldwide through intelligent connections in the life sciences and healthcare industries.
- • In this role, you will develop expertise in clinical trial operations, remote visit coordination, regulatory compliance (GCP, HIPAA), cross-functional communication, and project management while contributing to high-stakes decentralized trials that impact global health innovation.
🎯 Requirements
- • Bachelor’s degree (B.A./B.S.) from a four-year college or university or equivalent combination of education, training, and experience
- • Two (2) years of research experience strongly preferred
- • Strong written and verbal communication skills with good command of English and strong presentation skills
- • Excellent computer skills, proficient in MS Word, Excel, PowerPoint, and ability to master clinical trial database systems
- • Excellent organizational skills and strong attention to detail with proven ability to handle multiple tasks efficiently
- • Ability to adhere to FDA Good Clinical Practices, FDA regulations, SOPs, and Working Practice Documents for all clinical/non-clinical aspects of project implementation
🏖️ Benefits
- • Opportunity to work remotely (home-based in USA)
- • Exposure to global clinical research operations and decentralized trial execution
- • Professional development in regulatory compliance (GCP, HIPAA, ICH) and clinical trial systems
- • Role within a leading global provider of healthcare intelligence and clinical research services (IQVIA)
- • Potential base pay range of $51,000.00 - $127,400.00 when annualized
- • Access to health and welfare benefits and other forms of compensation (incentive plans, bonuses)
Skills & Technologies
About IQVIA Holdings Inc.
IQVIA Holdings Inc. provides advanced analytics, technology solutions, and clinical research services to the life-sciences industry. Formed through the 2016 merger of Quintiles and IMS Health, the company integrates healthcare data, analytics, and domain expertise to help biopharmaceutical and medical-device clients optimize drug development, commercialization, and real-world evidence generation. Its offerings span clinical trial design and execution, real-world insights, commercial strategy, and technology platforms that connect stakeholders across the healthcare ecosystem. Headquartered in Durham, North Carolina, IQVIA operates in more than 100 countries, supporting the development and delivery of therapies to improve patient outcomes worldwide.
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