Clinical Study Designer: EDC & Trial Logistics Lead

Celerion; Oklahoma; On-site; USD 28,000 - 29,000; Full time

Job summary

Celerion is seeking a Clinical Study Designer to join our Lincoln, Nebraska team. You will coordinate the logistical setup and ongoing maintenance of clinical trials using ClinQuick, ensuring accurate data capture and study conduct support.

The role requires an Associate’s degree in a health-related field or relevant experience, meticulous attention to detail, and the ability to thrive in a fast-paced environment, delivering timely, compliant trial documentation.

Qualifications

• Associate’s degree in a health-related field or applicable experience in medical/clinical settings.
• Detail-oriented, computer literate and able to work in a fast-paced atmosphere.
• Experience coordinating clinical trials and data capture workflows.

Responsibilities

• Logistical setup and ongoing maintenance of clinical trials in ClinQuick.
• Create study conduct manuals and instructions.
• Develop detailed timed event schedules for clinic staff and study participants.

Skills

Clinical trial coordination

EDC software

Detail oriented

Communication

Education

Associate’s degree in a health-related field

Tools

ClinQuick

Job description

Celerion is seeking a Clinical Study Designer to join our Lincoln, Nebraska team. You will coordinate the logistical setup and ongoing maintenance of clinical trials using ClinQuick, ensuring accurate data capture and study conduct support.

The role requires an Associate’s degree in a health-related field or relevant experience, meticulous attention to detail, and the ability to thrive in a fast-paced environment, delivering timely, compliant trial documentation.