Posted 9 days ago
Clinical Research Coordinator
IQVIAClinical Research Coordinator
Requirements
Vital signs collection, Phlebotomy, ECG conduction, Lab specimen processing, Site operations knowledge, CTMS proficiency, eCRF proficiency, Microsoft Office
Skills
Clinical ResearchPhlebotomyECGCTMS
About the role
Responsibilities
- Manage diverse clinical trials (typically 2–6) across multiple therapeutic areas
- Lead study coordination from start to finish, including patient recruitment and informed consent
- Perform essential clinical procedures including vital signs collection, phlebotomy, and ECG conduction
- Handle lab specimen processing and management
- Maintain regulatory documentation and prepare for site audits
- Collaborate closely with investigators, sponsors, and monitors
Requirements
- Experience in clinical skills: vital signs, phlebotomy, ECGs, and lab specimen processing
- Solid understanding of site operations and the drug development process
- CRC I level: 1-3 years of experience in a clinical research setting working with participants
- CRC II level: Minimum of 3 years of experience as a Clinical Research Coordinator
- Proficiency with CTMS, eCRF, and Microsoft Office tools
- Strong written and verbal communication skills with high attention to detail
About the Company
IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. Through our work with Avacare, a dynamic Site Management Organization (SMO), we create intelligent connections to accelerate the development and commercialization of innovative medical treatments to improve patient outcomes worldwide.
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IQVIA · Elkhorn
