Clinical Research Coordinator I — Multi-Trial Experience

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

Job summary

Avacare, an SMO in Elkhorn, Nebraska, seeks Clinical Research Coordinators to support multiple trials on-site. You will handle recruitment, informed consent, regulatory docs, and study coordination in a collaborative team environment.

You will gain exposure to diverse protocols, lead trial activities, and develop regulatory and operational skills for future roles in clinical operations and monitoring.

Qualifications

• Hands-on skills: vital signs, phlebotomy, ECGs, processing lab specimens.
• Solid understanding of site operations and the drug development process.
• CRC experience: CRC I (1–3 years) or CRC II (3+ years) at a clinical investigative site.
• Strong written and verbal communication with good time management.

Responsibilities

• Manage 2–6 trials of varying complexity from start to finish.
• Recruit patients and obtain informed consent; maintain regulatory documentation.
• Coordinate study activities and ensure site audits readiness.
• Collaborate with investigators, sponsors and monitors.

Skills

Vital signs

Phlebotomy

ECGs

Lab specimens

Site operations

Communication & documentation

CTMS

eCRFs

MS Office

Tools

CTMS

eCRFs

MS Office

Job description

Avacare, an SMO in Elkhorn, Nebraska, seeks Clinical Research Coordinators to support multiple trials on-site. You will handle recruitment, informed consent, regulatory docs, and study coordination in a collaborative team environment.

You will gain exposure to diverse protocols, lead trial activities, and develop regulatory and operational skills for future roles in clinical operations and monitoring.