Clinical Research Coordinator

About the role

This position is responsible for coordinating various trial activities including preparing and submitting regulatory submissions to IRB and sponsors, ensuring documentation compliance for multiple study projects, preparing audit materials, and submitting data.

Responsibilities

• Prepares and submits regulatory submissions to IRB and sponsors
• Documentation compliance for multiple study projects
• Audit preparation
• Data submission
• Advising patients on trial design
• Facilitating informed consent for investigators
• Following strict adherence to protocol procedures specific to each study
• Screwing for possible trial patients, eligibility criteria, and patient follow-up

Requirements

• Research certification within one year of eligibility
• Minimum of five years of healthcare experience with two years in a research role
• Completion of Good Clinical Practice & Human Subject Protection and Safety Handling/Hazardous training within two weeks of hire/transfer date

Preferred Qualifications

• In-depth knowledge of good clinical practices as set forth by Federal regulations
• An organized individual with strong critical thinking skills who can work efficiently under pressure
• Highly motivated, proactive, and able to work independently as well as in a team

Education

• A D: Associate's Degree preferred
• B D: Bachelor Degree preferred