Research Coordinator-Cardiology

Gbh Glenbrook Hospital Glenviewmid

OtherResearch Coordinator

0 views0 saves0 applied

Apply Now

Quick Summary

Key Responsibilities

Prepare sites for conducting the study, including assisting PIs with feasibility assessments Develop Standard Operating Procedures Develop study forms,

Technical Tools

OtherResearch Coordinator

$24.86 - $37.29 - The hourly pay rate offered is determined by a candidate's expertise and years of experience, among other factors.

Position: Research Coordinator, Cardiology
Location: Glenview, IL
Full Time
Hours: Monday-Friday, 8:00am-4:30pm

Responsibilities

~2 min read

→Prepare sites for conducting the study, including assisting PIs with feasibility assessments
→Develop Standard Operating Procedures
→Develop study forms, necessary database programs & data collection/entry strategies with applicable staff
→Train medical assistants and nurses with regard to study protocols
→Review & prepare correspondence with the Endeavor IRB (initial submission, protocol amendments, adverse events, yearly progress reports, etc)
→Maintain regulatory documents as per sponsor & IRB protocols
→Screen subjects for eligibility
→Responsible for recruitment, coordination of care (in compliance with study protocol), and retention of research subjects
→Participate in the Informed Consent process
→Complete study activities as dictated by research protocols (including face to face and telephone assessments, medical records abstraction, etc.)
→Responsible for specimen collection, processing, and shipping (as applicable)
→Coordinate & schedule appointments for diagnostic tests & procedures associated w/study protocols
→Responsible for completing & maintaining CRF’s & source documentation
→Follow proper subject billing procedures
→Manage payments to study subjects
→Complete study close-out activities for each study and follow appropriate archiving/storing/retention procedures and policies

→Education: High School Diploma Required; Bachelor's degree preferred
→Experience: 1-2 years minimum experience as a Research Assistant or Research Coordinator in human subjects research (or equivalent position) required. Experience facilitating recruitment and follow up strategies with subjects’/clinic personnel, operational problem solving and ability to manage complex clinical trials with minimal supervision