Job Description

Highlights

• $50,000 - $60,000 salary + benefits!
• Consistent schedule, no overnights or weekends, flex holidays, and more!
• Work with a company that truly cares about their employees and patients

About Our Client

Our client is a long standing clinical research site in the Columbus, OH area that takes a truly unique patient-centric, service-oriented, approach to clinical research. Their reputation for excellence has been built across over 20 therapeutic areas, over 15 physicians, and over 550 completed trials! They are looking to expand their team with a skilled clinical research coordinator!

Responsibilities

As a CRC you will be a specialized research professional under the direction of the clinical Principal Investigator and Site Manager. While the PI and Site Manager are responsible for the overall design, conduct, and management of the clinical trial, you support, facilitate, and coordinate the daily clinical trial activities and play a critical role in the conduct of the study including supporting patients throughout the clinical trial process!

• Conduct procedures such as vital signs, blood draws, EKGs, and bladder scans.
• Patient recruitment, enrollment, scheduling, and consent
• Lab procedures and shipments
• Maintain GCP and follow protocols
• Data management in EDC systems
• Overall coordination of the study

Qualifications:

• 2+ years of experience working as a CRC on sponsor backed clinical trials
• Phlebotomy and lab processing experience (ability to perform without supervision)
• Ability to work on site M-F on site (there is no remote or hybrid days)

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