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Cleveland Clinic Health System is seeking a Research Coordinator I for the Neuro GI team at the Cleveland Clinic Main Campus. You will enroll patients in clinical trials, conduct visits, collect data, obtain physician signatures, and support biorepository activities in a fast-paced, patient-centered environment.
Responsibilities include regulatory maintenance, IRB submissions, adverse event reporting, and collaboration with investigators and sponsors to ensure protocol execution and study
Research Coordinator I NE - Neuro GI
Cleveland
Cleveland Clinic Main Campus
DDSI Clinical Research Unit-Digestive Disease Institute
D99967
Days
8:00am-5:00pm
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 supporting the Neuro GI team, your role is crucial in enrolling patients in clinical trials, conducting study visits and collecting questionnaires with important study-related information. In this role, you will obtain physician signatures, assist with minimal-risk studies and support biorepository activities. Whilenumerousresponsibilities can be difficult to juggle at times, your team will encourage you to enhance your skills and improve your ability toidentifynew avenues of treatment. Come join a culture devoted to pushing the needle forward in healthcare.
A caregiver in this position works days from 8:00 a.m. – 4:30 p.m. (flexible start/end times)
A caregiver who excels in this role will:
Assistwith coordinating the compliant implementation and conduct of human subject research projects.
Maintain regulatory documents and binders, conduct data management, complete IRBsubmissionsand communicate with the research team.
Report and complete serious adverse events and/or safety logs.
Communicate with sponsors,monitorsand research personnel to ensure all aspects of study compliance.
Collaborate with primary investigators,sponsorsand research caregivers to plan,conductand evaluate project protocols, including research subject recruitment.
Schedule pre-site selection visits, site initiation visits, webinars,monitoringand 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, monitoringplansand protocol-related activities.
Assistwith preparing and responding to audits andmaintainingresearch tools.
Complete certification in Human Subjects Research as required by the Responsible Conduct of Research guidelines adopted by Cleveland Clinic.
Minimum qualifications for the ideal future caregiver include:
HighSchoolDiploma or GEDand two years of clinical research or healthcare experience
ORAssociate’s or Bachelor’sDegree in a healthcare or a science-related field
Demonstratedproficiencywith various computer-based skills (word processing, spreadsheets, databases, presentation software, data entry, and EPIC)
Understanding of the basic concepts of study design
Within90 daysof hire,mustsuccessfully complete certification in Human Subjects Research as required by the Responsible Conduct of Research guidelines adopted by Cleveland Clinic
Strong organizational,communicationand interpersonal skills
Preferred qualifications for the ideal future caregiver include:
Associate’s orBachelor’sDegree inahealthcare or a science-related field
Previous STNA/bench research experience
Experience with Microsoft Office Suite and EPIC
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.