On-Site CRC I: Lead Diverse Trials & Grow Your Career

IQVIA Argentina; Fremont (CA); On-site; USD 38,000 - 95,000; Full time

Job summary

IQVIA is seeking Clinical Research Coordinators for an on-site position in Elkhorn, Nebraska. The role involves patient recruitment, informed consent, and comprehensive trial coordination across multiple therapeutic areas.

You will work closely with investigators, sponsors, and monitors to ensure protocol compliance and quality data capture. Ideal candidates have hands-on clinical skills, strong communication, and proficiency with CTMS/eCRFs and MS Office.

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.

Responsibilities

• Recruit and enroll participants across trials and obtain informed consent.
• Manage regulatory documentation and perform site audits.
• Coordinate study activities across multiple therapeutic areas and lead trial coordination from start to finish.
• Collaborate with investigators, sponsors, and monitors to ensure protocol compliance.

Skills

Clinical Skills

Site Operations

Communication

Documentation

Time Management

Technical Proficiency

Tools

CTMS

eCRFs

Microsoft Office

Job description

IQVIA is seeking Clinical Research Coordinators for an on-site position in Elkhorn, Nebraska. The role involves patient recruitment, informed consent, and comprehensive trial coordination across multiple therapeutic areas.

You will work closely with investigators, sponsors, and monitors to ensure protocol compliance and quality data capture. Ideal candidates have hands-on clinical skills, strong communication, and proficiency with CTMS/eCRFs and MS Office.