Clinical Research Coord II

University of Florida • Gainesville, FL

37d • $53,000 - $59,800

About The Position

Manage assigned human subjects research studies including but not limited to: recruitment, review of eligibility criteria, patient screening, facilitate informed consent, maintain accurate study records, collect data, update OnCore, coordinate communication for the study team, act as the liaison for the research participant and work collaboratively to ensure all study activities are completed. Perform detailed chart review, input data, resolve data queries in a timely fashion, schedule monitor visits, schedule patient visits, maintain consistent communication at regular/frequent intervals with PI and study team, maintain regulatory binders and patient binders, maintain good working relationships with nursing staff, facilitate trainings on protocols as directed, work on special projects as needed, conduct literature reviews, create bibliographies as needed, assist with data analysis on specific projects as needed. Write, edit, and/or submit IRBs for new projects and ensure IRB compliance for current projects. Write edit and submit ICF's and ensure IRB compliance, work with startup team to assist with site activation as needed. Assist with other research, education or administrative related tasks as needed.

Requirements

• Bachelor's degree in an appropriate area and two years of relevant experience; or an equivalent combination of education and experience.

Nice To Haves

• 1 - 2 years human subjects research experience
• Previous clinical trials experience
• Clinical or direct patient contact experience
• Previous lab experience
• Able to work collaboratively, forward ideas as appropriate and problem solve when needed
• Multi-media capabilities strongly preferred; proficiency with Microsoft Office such as Word, PowerPoint and Excel.

Responsibilities

• Manage assigned human subjects research studies including but not limited to: recruitment, review of eligibility criteria, patient screening, facilitate informed consent, maintain accurate study records, collect data, update OnCore, coordinate communication for the study team, act as the liaison for the research participant and work collaboratively to ensure all study activities are completed.
• Perform detailed chart review, input data, resolve data queries in a timely fashion, schedule monitor visits, schedule patient visits, maintain consistent communication at regular/frequent intervals with PI and study team, maintain regulatory binders and patient binders, maintain good working relationships with nursing staff, facilitate trainings on protocols as directed, work on special projects as needed, conduct literature reviews, create bibliographies as needed, assist with data analysis on specific projects as needed.
• Write, edit, and/or submit IRBs for new projects and ensure IRB compliance for current projects. Write edit and submit ICF's and ensure IRB compliance, work with startup team to assist with site activation as needed.
• Assist with other research, education or administrative related tasks as needed.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Industry: Educational Services
• Number of Employees: 5,001-10,000 employees