Clinical Research Coordinator

Description

• Ensure the safety of subjects during the study.
• Educate subjects on protocols, study interventions, and study drugs.
• Maintain and organize study source documents; report adverse events promptly.
• Ensure data collected is accurate, legible, and organized according to GCP.
• Coordinate day-to-day activities of research visits, including vital signs, EKG, phlebotomy, and lab work assessments.
• Ensure subjects participating in clinical trials follow the study protocol as directed.
• Develop strong working relationships and maintain effective communication with study team members.

Requirements

• Clinical Research Coordinator experience (minimum 2 years).
• Understanding of study drug background and study requirements.
• Proficiency with MS Office suite (Outlook, Word, Excel, PowerPoint, SharePoint) and clinical trial master filing systems.
• Proficiency in Good Clinical Practice (GCP).
• Phlebotomy skills and experience with EKG and injections.

Benefits

• Health Spending Account (HSA)
• Transportation benefits
• Life Insurance (Voluntary Life & AD&D for the employee and dependents)
• 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
• Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in OMAHA,NE. Application Deadline This position is anticipated to close on Jan 12, 2026.
• Critical Illness, Accident, and Hospital
• Short and long-term disability
• Employee Assistance Program
• Medical, dental & vision

Training + Development

Interview process

Visa Sponsorship

Security clearance