Research Coordinator I – Dasarathy Lab

Cleveland Clinic•Cleveland, OH

2d•Onsite

About The Position

At Cleveland Clinic Health System, we believe in a better future for healthcare. And each of us is responsible for honoring our commitment to excellence, pushing the boundaries and transforming the patient experience, every day. We all have the power to help, heal and change lives — beginning with our own. That’s the power of the Cleveland Clinic Health System team, and The Power of Every One. Join Cleveland Clinic’s Main Campus where research and surgery are advanced, technology is leading-edge, patient care is world class and caregivers are family. Here, you will work alongside a passionate and dedicated team, receive endless support and appreciation, and build a rewarding career with one of the most respected healthcare organizations in the world. Innovative research and groundbreaking discoveries happen every day at Cleveland Clinic. Each member of our team contributes to our mission of caring for life, researching health and educating those who serve. We’re creating an environment of belonging - where everyone is valued and respected - dedicated to collaboration, mentorship, diversity and inclusion. Click the line to learn more about our Dasarathy Lab: https://www.lerner.ccf.org/inflammation-immunity/dasarathy/ A caregiver in this position works from 8:00am – 5:00pm.

Requirements

High school diploma or GED
Two years of clinical research or healthcare experience
Demonstrated proficiency with various computer-based skills (word processing, spreadsheets, databases, presentation software, data entry, and EPIC
Understanding of the basic concepts of study design

Nice To Haves

Associate’s or bachelor’s degree in healthcare or a science-related field. This may substitute for two years of the experience requirement

Responsibilities

Assist with coordinating the compliant implementation and conduct of human subject research projects, typically of low workload and low complexity.
Maintain regulatory documents and binders, conduct data management, complete IRB submissions and communicate with the research team.
Report and complete serious adverse events and/or safety logs.
Communicate with sponsors, monitors and research personnel to ensure all aspects of study compliance.
Collaborate with primary investigators, sponsors and research caregivers to plan, conduct and evaluate project protocols, including research subject recruitment.
Schedule pre-site selection visits, site initiation visits, webinars, monitoring and close-out visits.
Plan, conduct and evaluate project protocols and research subject recruitment.
Monitor and report project status and research data.
Complete regulatory documents, data capture, monitoring plans and protocol-related activities.
Assist with preparing and responding to audits and maintaining research tools.
Complete certification in Human Subjects Research as required by the Responsible Conduct of Research guidelines adopted by Cleveland Clinic.