On-Site Clinical Research Coordinator I — Start Your Trials

IQVIA Argentina; Elkhorn (WI); On-site; USD 38,000 - 95,000; Full time

Job summary

Avacare, an IQVIA business, is seeking a Clinical Research Coordinator for a fully on-site role in Elkhorn. The CRC will handle patient recruitment, informed consent, regulatory documentation, and site audits within a dynamic SMO environment.

Ideal candidates have hands-on clinical skills and knowledge of site operations, with 1–3 years CRC experience for CRC I or 3+ years for CRC II, plus proficiency in CTMS, eCRFs, and Microsoft Office.

Qualifications

• Hands-on experience in vital signs, phlebotomy, ECGs, and processing lab specimens.
• Solid understanding of site operations and the drug development process.
• CRC I: 1-3 years in a clinical research site; CRC II: 3 years as a CRC.
• Strong written and verbal communication with attention to detail and time management.
• Proficient with CTMS, eCRFs, and Microsoft Office.

Responsibilities

• Manage patient recruitment and informed consent from start to finish.
• Regulatory documentation and site audit responsibilities.
• Lead study coordination across multiple trials and collaborate with investigators, sponsors, and monitors.

Skills

Clinical Skills

Site Operations Knowledge

Communication & Documentation

Technical Proficiency

Tools

CTMS

eCRFs

Microsoft Office

Job description

Avacare, an IQVIA business, is seeking a Clinical Research Coordinator for a fully on-site role in Elkhorn. The CRC will handle patient recruitment, informed consent, regulatory documentation, and site audits within a dynamic SMO environment.

Ideal candidates have hands-on clinical skills and knowledge of site operations, with 1–3 years CRC experience for CRC I or 3+ years for CRC II, plus proficiency in CTMS, eCRFs, and Microsoft Office.