Research Coordinator II - Neurological Institute

Cleveland Clinic; Cleveland (OH); In loco; USD 56.000 - 76.000; Tempo pieno

Descrizione del lavoro

Cleveland Clinic is seeking a Research Coordinator II for the Neurological Institute at the Main Campus in Cleveland, OH. The role supports the Cerebrovascular Center’s research program by enrolling patients, conducting visits, and collecting data for clinical trials. This onsite position includes on-call coverage, with a schedule from 8:00 a.m.

to 5:00 p.m. and remote work up to one day per week after the initial period.

Competenze

• High School Diploma or GED and 3 years as Research Coordinator I, or health/science degree with 1 year experience as RC I.
• Proficient with word processing, spreadsheets, database and presentation software.
• Preferred: Associate or bachelor’s degree in health care or science related field.

Mansioni

• Coordinate and conduct study activities including regulatory document management, IRB submissions, and data collection/entry.
• Communicate with sponsors, monitors, and research personnel to ensure study compliance.
• Assist with study visits, including scheduling of pre-site selection, initiation, monitoring, webinars, and close-out visits.
• Collaborate with investigators, sponsors, and staff on protocol development, execution, and evaluation, including subject recruitment.
• Report and document Serious Adverse Events, safety logs, FDA/sponsor forms, and project status.
• Maintain regulatory binders, monitoring plans, and personnel certification records (e.g., licenses, CVs, CITI training).
• Support preparation for and response to audits.
• Develop and maintain study-related tools such as tracking spreadsheets and educational materials.
• Monitor data quality and protocol adherence; demonstrate understanding of study design and protocol requirements.

Conoscenze

Regulatory documentation

Clinical coordination

Data collection

Formazione

High School Diploma or GED

Associate or Bachelor’s in health care or science

Strumenti

Word processing

Spreadsheets

Database software

Presentation software

Descrizione del lavoro

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 II - Neurological Institute

Location

Cleveland

Facility

Cleveland Clinic Main Campus

Department

Cerebrovascular Center-Neurological Institute

Job Code

T99498

Shift

Days

Schedule

8:00am-5:00pm

Job Summary

Job Details

Join Cleveland Clinic’s Neurological Institute and become a part of one of the most respected healthcare organizations in the world. Cleveland Clinic is recognized as one of the top hospitals in the nation. The Neurological Institute is known for being a leader in treating and researching the most complex neurological disorders and advancing innovations in neurology.

Groundbreaking research and 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. As Research Coordinator II, you will play a vital role in supporting the Cerebrovascular Center’s research program by enrolling patients into clinical trials, conducting study visits and collecting questionnaires with critical study-related data. While the numerous responsibilities can be difficult to juggle at times, your team will encourage you to enhance your skills and improve your ability to identify new 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. – 5:00 p.m.

This position requires on-call coverage approximately one week per month, with hours from 5:00 p.m.–11:00 p.m. Monday through Friday and 7:00 a.m.–11:00 p.m. on Saturday and Sunday.

This role is based on-site at Main Campus four days per week, with the option to work remotely one day per week following the initial hiring period.

A caregiver who excels in this role will:

• Coordinate and conduct study activities including regulatory document management, IRB submissions, and data collection/entry.

• Communicate with sponsors, monitors, and research personnel to ensure study compliance.

• Assist with study visits, including scheduling of pre-site selection, initiation, monitoring, webinars, and close-out visits.

• Collaborate with investigators, sponsors, and staff on protocol development, execution, and evaluation, including subject recruitment.

• Report and document Serious Adverse Events, safety logs, FDA/sponsor forms, and project status.

• Maintain regulatory binders, monitoring plans, and personnel certification records (e.g., licenses, CVs, CITI training).

• Support preparation for and response to audits.

• Develop and maintain study-related tools such as tracking spreadsheets and educational materials.

• Monitor data quality and protocol adherence; demonstrate understanding of study design and protocol requirements.

Minimum qualifications for the ideal future caregiver include:

• High School Diploma or GED and three years of experience as a Research Coordinator I or performing the role of a Research Coordinator I OR Associate’s or Bachelor’s degree in health care or science related and one year of experience as a Research Coordinator I or performing the role of a Research Coordinator I

• Proficient with computer-based skills such as word processing, spreadsheets, database and presentation software

Preferred qualifications for the ideal future caregiver include:

• Associate or bachelor’s degree in health care or science related field

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.