Clinical Research Coordinator I

About the role

This is a fully on-site position in Elkhorn, Nebraska. Are you ready to accelerate your career in clinical research? Join Avacare, a dynamic Site Management Organization (SMO) where Clinical Research Coordinators (CRCs) gain unparalleled exposure to diverse trials, hands-on responsibilities, and a collaborative team environment.

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.