Clinical Research Coordinator
IQVIA
Summary
This is a fully on-site position in Las Vegas, Nevada. Join Avacare, a dynamic Site Management Organization (SMO) where Clinical Research Coordinators (CRCs) gain unparalleled exposure to diverse trials, hands-on responsibilities, and a collaborative team environment.
Job description
Why Avacare?
At Avacare, CRCs wear more hats than in traditional research settings. You'll gain experience across multiple therapeutic areas, manage complex protocols, and take ownership of key trial activities — from patient recruitment and informed consent to regulatory documentation and site audits. This breadth of responsibility not only strengthens your core CRC skills but also prepares you for future roles in clinical operations, monitoring, and beyond.
What You'll Gain
- Broadened Skill Set: Manage 2–6 trials of varying complexity, perform clinical procedures, and lead study coordination from start to finish.
- Professional Growth: Work closely with investigators, sponsors, and monitors while mentoring junior staff and contributing to internal training.
- Collaborative Culture: Be part of a supportive team that values initiative, adaptability, and continuous learning.
- Global Impact: Experience the synergy of working within a local SMO backed by the resources and reach of a global CRO.
Qualifications
- Clinical Skills: Hands-on experience in obtaining vital signs, performing phlebotomy, conducting ECGs, and processing lab specimens.
- Site Operations Knowledge: Solid understanding of site operations and the drug development process.
Experience
- CRC I: Minimum of 1-3 years in clinical research setting at a clinical investigative site working with participants.
- CRC II: Minimum of 3 years as a Clinical Research Coordinator in a clinical investigative site working with participants.
- Communication & Documentation: Strong written and verbal communication skills, with attention to detail and time management.
- Technical Proficiency: Comfortable using CTMS, eCRFs, and Microsoft Office tools.
Requirements
- Hands-on experience in obtaining vital signs, performing phlebotomy, conducting ECGs, and processing lab specimens
- Solid understanding of site operations and the drug development process
- CRC I: Minimum of 1-3 years in clinical research setting at a clinical investigative site working with participants
- CRC II: Minimum of 3 years as a Clinical Research Coordinator in a clinical investigative site working with participants
- Strong written and verbal communication skills, with attention to detail and time management
- Comfortable using CTMS, eCRFs, and Microsoft Office tools
Benefits
- Health and welfare benefits
Company overview
IQVIA is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. Headquartered in Durham, North Carolina, the company operates in over 100 countries with approximately 86,000 employees worldwide. IQVIA specializes in creating intelligent connections across all aspects of healthcare through its proprietary IQVIA Connected Intelligence platform, which combines analytics, transformative technology, big data resources, and extensive domain expertise. The company's comprehensive portfolio includes clinical trial management, real-world evidence generation, commercial insights, and regulatory compliance services. IQVIA serves a diverse client base including pharmaceutical manufacturers, biotechnology companies, medical device firms, government agencies, and healthcare providers. With its Healthcare-grade AI capabilities and extensive global data assets, IQVIA accelerates the development and commercialization of innovative medical treatments while improving healthcare outcomes for patients globally. The company is publicly traded on the New York Stock Exchange under the ticker symbol IQV.