Clinical Study Designer: Trial Setup & Manuals

Celerion Holdings, Inc.; Lincoln (NE); On-site; USD 60,000 - 80,000; Full time

Job summary

Celerion Holdings, Inc. is seeking a full-time Clinical Study Designer at our Lincoln, Nebraska location. In this role, you will be responsible for the logistical setup and maintenance of clinical trials using ClinQuick, our electronic data capture system.

The ideal candidate will have an Associate’s degree in a health-related field or relevant experience, be detail-oriented, and able to thrive in a fast-paced environment. Join our committed team in helping bring innovative drugs to market faster.

Qualifications

• Associate’s degree in a health-related field or applicable experience in a medical, clinical, pharmaceutical, or laboratory setting.
• Detail-oriented and computer literate.

Responsibilities

• Responsible for the logistical set up and maintenance of clinical trials.
• Manage the creation of study conduct instruction manuals.
• Create detailed timed event schedules for clinic staff and study participants.

Skills

Detail-oriented

Computer literate

Ability to work in a fast-paced atmosphere

Education

Associate’s degree in a health-related field

Job description

Celerion Holdings, Inc. is seeking a full-time Clinical Study Designer at our Lincoln, Nebraska location. In this role, you will be responsible for the logistical setup and maintenance of clinical trials using ClinQuick, our electronic data capture system.

The ideal candidate will have an Associate’s degree in a health-related field or relevant experience, be detail-oriented, and able to thrive in a fast-paced environment. Join our committed team in helping bring innovative drugs to market faster.