
Research Coordinator I NE - Tang Lab
Cleveland, OHFull-timePosted 1 day agoStill listed today
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Job overview
The Research Coordinator I in the Tang Lab supports human-subject research focused on heart failure and cardiomyopathy. The role involves coordinating clinical studies, enrolling and interacting with patients, conducting study visits and research procedures, and managing regulatory documents and data. The coordinator works with investigators, sponsors, monitors, and research personnel to support study compliance and contribute to cardiovascular research.
Skills & qualifications
Skills
Qualifications
Full job description
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.
Job Title Research Coordinator I NE - Tang Lab Location Cleveland Facility Cleveland Clinic Main Campus Department RES Heart Blood and Kidney Research-Research Innov and Educ Job Code D99967 Shift Days Schedule 8:30am-5:00pm Job Summary
Job Details
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.
The Tang Lab focuses on advancing precision cardiovascular research by investigating the underlying biological mechanisms of heart failure and cardiomyopathy. Through clinical studies, advanced cardiovascular phenotyping, molecular biology, genomics, biomarker discovery, and translational research, the lab aims to improve early disease detection, risk stratification, and the development of targeted therapies to improve patient outcomes. As a Research Coordinator I, you will play an important role in enrolling patients in clinical trials, conducting study visits, collecting questionnaires, and performing research-related procedures. In this role, you will interact directly with patients throughout the screening, enrollment, and study visit processes, helping increase their understanding of their disease and the impact of research on future patient care. You will have opportunities to enhance your research skills and contribute to identifying new avenues for treatment. Read more about the Tang lab: https://www.lerner.ccf.org/heart-blood-kidney/tang/
A caregiver in this position works days from 8:30 a.m. – 5:00 p.m. (flexible)
A caregiver who excels in this role will:
- 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 visits, 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 for and responding to audits and maintaining research tools.
- Screen patients for study eligibility based on established inclusion and exclusion criteria.
- Discuss research studies with patients and obtain informed consent for participation.
- Perform phlebotomy for research purposes.
- Process blood and urine research samples (training provided).
- Perform various study procedures, including questionnaire administration, vital signs assessment, and EKGs (training provided).
- Maintain study regulatory binders.
Minimum qualifications for the ideal future caregiver include:
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High School Diploma or GED and two years of clinical research or healthcare experience
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OR Associate’s or Bachelor’s Degree in a healthcare or a science-related field
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Demonstrated proficiency with various computer-based skills (word processing, spreadsheets, databases, presentation software, data entry, and EPIC)
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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
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Strong organizational, communication and interpersonal skills
Preferred qualifications for the ideal future caregiver include:
- Associate’s or Bachelor’s Degree in a healthcare or a science-related field
- Phlebotomy certified
Physical Requirements:
- Ability to perform work in a stationary position for extended periods
- Ability to operate a computer and other office equipment
- Ability to communicate and exchange accurate information
- In some locations, ability to move up to 25 pounds
Personal Protective Equipment:
- Follows standard precautions using personal protective equipment as required.
The policy of Cleveland Clinic Health System and its system hospitals (Cleveland Clinic Health System) is to provide equal opportunity to all of our caregivers and applicants for employment in our drug free environment. All offers of employment are followed by testing for controlled substances.
Cleveland Clinic Health System 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.
Decisions concerning employment, transfers and promotions are made upon the basis of the best qualified candidate without regard to color, race, religion, national origin, age, sex, sexual orientation, marital status, ancestry, status as a disabled or Vietnam era veteran or any other characteristic protected by law. Information provided on this application may be shared with any Cleveland Clinic Health System facility.
If applying for a Florida position, please see the following website for more information on the background screening requirements required by the Agency of Health Care Administration: https://info.flclearinghouse.com/
Please review the Equal Employment Opportunity poster.
Cleveland Clinic is pleased to be an equal employment opportunity employer.
How this job compares
Set against the 1,179 open Clinical Research jobs on Olive Jobs, counted November 3, 2026.
- Pay
- This postingNot listed
- US median$119–195K/yr573 salary ranges
- US median$25–35/hr162 hourly ranges
- Openings
- Olive Jobs lists 36 open Clinical Research jobs in Ohio and 1,179 across the US. 12% of them nationwide are listed as remote or flexible.
- Hiring the most in Ohio
- Cleveland Clinic (this employer)16 open
- University Hospitals Health System4 open
- CommonSpirit Health at Home3 open
- Experience
- Clinical Research postings that state a minimum ask for 3 years of experience at the median; the middle half ask for 2 to 5 years (841 postings).
- Education
- 456 of the 1,179 open Clinical Research jobs (39%) ask for a bachelor's degree or higher.
Counted across the open, public US postings on Olive Jobs on November 3, 2026. Pay medians are the middle values of the low ends and of the high ends of postings that list both ends of a range in the same cadence (a yearly salary or an hourly rate); a range's midpoint is halfway between its ends. Pay and experience figures resting on fewer than 20 postings are left out.
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