Research Coordinator I NE

Cleveland Clinic • Cleveland, OH

2d • Onsite

About The Position

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. As a Research Coordinator I for the Lymphoma Research Group, you will play a crucial role in enrolling patients in clinical trials, conducting study visits, and collecting questionnaires containing important study-related information. In this role, you will support lymphoma research studies throughout various stages of the trial, including study start-up, maintenance, and closeout activities. Your responsibilities will include data entry, study closeout tasks, meetings, and frequent communication through Microsoft Teams, with day-to-day priorities driven by email and incoming study needs. You will have a particular focus on T-cell lymphoma research, helping expand this area of the research portfolio while supporting the growth of the data registry. While balancing multiple responsibilities can be challenging, your team will encourage you to develop your skills and strengthen your ability to identify new avenues for treatment. Join a team committed to advancing healthcare and pushing the needle forward in lymphoma research.

Requirements

• High School Diploma or GED and two years of clinical research or healthcare experience OR Associate’s or Bachelor’s Degree in a healthcare or a science-related field
• 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
• Within 90 days of hire, must successfully complete certification in Human Subjects Research as required by the Responsible Conduct of Research guidelines adopted by Cleveland Clinic
• Strong organizational, communication and interpersonal skills

Nice To Haves

• Associate’s or Bachelor’s Degree in a healthcare or a science-related field
• Clinical research trial experience (data, regulatory)

Responsibilities

• Assist with coordinating the compliant implementation and conduct of human subject research projects.
• 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.

Benefits

• Follows standard precautions using personal protective equipment as required.
• Administers an influenza prevention program. You will be required to comply with this program, which will include obtaining an influenza vaccination on an annual basis or obtaining an approved exemption.

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level
• Education Level: High school or GED