Clinical Research Coordinator I (Clinical Research)

Location: Fully onsite in Elkhorn, Nebraska, United States

Salary: $37,800–$94,500 annualized base pay, depending on qualifications, location, and schedule.

Company

IQVIA provides clinical research services, commercial insights, and healthcare intelligence for the life sciences and healthcare industries.

What you will do

• Coordinate 2–6 clinical trials with varying levels of complexity.
• Manage study activities from patient recruitment and informed consent through trial completion.
• Perform vital signs, phlebotomy, ECGs, and laboratory specimen processing.
• Maintain regulatory documentation and support site audits.
• Collaborate with investigators, sponsors, and clinical monitors.
• Contribute to internal training and mentor junior staff.

Requirements

• Minimum 1–3 years of experience in a clinical research setting at an investigative site working with participants.
• Hands-on experience obtaining vital signs, performing phlebotomy, conducting ECGs, and processing laboratory specimens.
• Solid understanding of site operations and the drug development process.
• Strong written and verbal communication, attention to detail, and time-management skills.
• Comfort using CTMS, eCRFs, and Microsoft Office tools.
• Ability to work fully onsite in Elkhorn, Nebraska.

Culture & Benefits

• Exposure to diverse clinical trials and multiple therapeutic areas within a Site Management Organization.
• Hands-on responsibility and opportunities for continuous learning and professional growth.
• Collaboration within a local SMO supported by the resources and reach of a global CRO.
• Health, welfare, and other benefits may be available depending on the position offered.
• Potential incentive plans, bonuses, or other additional compensation may be offered.