Research Coordinator III - Ophthalmology Retina/Uveitis at Cleveland Clinic

, , United States -

Full Time

Start Date

Immediate

Expiry Date

02 May, 26

Salary

0.0

Posted On

01 Feb, 26

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Clinical Trials, Patient Care, Data Entry, Regulatory Compliance, Research Protocols, IRB Submissions, Patient Recruitment, Adverse Event Reporting, Collaboration, Project Management, Communication, Research Design, Quality Assurance, Documentation, Phlebotomy, Testing

Industry

Hospitals and Health Care

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 III - Ophthalmology Retina/Uveitis Location Cleveland Facility Cleveland Clinic Main Campus Department Cole Eye Research-Main Campus Hospital Job Code T99497 Shift Days Schedule 7:30am-4:00am 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 Research Coordinator III is embedded within the clinical research department and supports clinical trials across multiple ophthalmology subspecialties including glaucoma, cornea, ocular oncology, neuro-ophthalmology and plastics. This role collaborates closely with physicians, sponsors and monitors to support the successful conduct of research studies. Responsibilities include screening, enrolling and consenting patients for clinical trials, preparing and maintaining IRB submissions and sponsor-required regulatory binders, ensuring readiness for monitoring visits and audits and collecting and entering study data in accordance with protocol requirements while maintaining HIPAA and research compliance. The coordinator also schedules patient visits, manages investigational drug and device trials and supports special projects including multi-center studies and investigation into new drug and device protocols. A caregiver in this position works between 7:30am to 4:00pm. A caregiver who excels in this role will: Demonstrate exceptional coordination and compliance of the implementation and conduct of human subject research projects. Assist with research study design and protocol development as applicable. Independently direct large, complex, multi-center clinical research protocols/programs and coordinate the implementation and conduct of research projects, ensuring adherence to research protocol. Report Serious Adverse Events and/or safety as they occur and complete Food and Drug Administration (FDA) and sponsor forms in accordance with GCP guidelines. Communicate with sponsors, monitors and research personnel to ensure all aspects of study compliance. Serve as a liaison between investigators, research personnel, outside study personnel and central research administration offices to assist in protocol interpretation, enrollment and safety questions. Collaborate with primary investigators, sponsors and research caregivers to plan, conduct and evaluate project protocols, including research subject recruitment. Monitor and report project status. Complete regulatory documents, data capture and monitoring plans. Complete and oversee protocol related activities. As delegated, attain and maintain clinical competencies for unlicensed caregivers, such as phlebotomy, vital signs, ECG, POC testing and other testing as required. Oversee and monitor research data to maintain quality. Develop and maintain knowledge of research protocols to coordinate the comprehensive and compliant execution of assigned protocols. Assist with the preparation for audits and response to audits. Develop or assist in the development and maintenance of research tools, such as spreadsheets, questionnaires and/or brochures. Maintain study personnel certification records (License, CV, CITI). Conduct and document the informed consent process. Assist the PI with research study design and development of research protocol. Submit the study to appropriate agencies in support of the research programs and assist with annual and other reporting requirements. Contribute to or assist with research project budget development. Minimum qualifications for the ideal future caregiver include: High School Diploma or GED and five years of experience as a Research Coordinator II or performing the role of a Research Coordinator II OR Bachelor’s Degree in a healthcare or science-related field and three years of experience Demonstrated proficiency with a variety of computer-based skills (word processing, spreadsheets, databases and presentation software) Understanding of the basic concepts of study design Preferred qualifications for the ideal future caregiver include: Associate’s or Bachelor’s Degree in a healthcare 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. Please review the Equal Employment Opportunity poster. Cleveland Clinic Health System is pleased to be an equal employment employer: Women / Minorities / Veterans / Individuals with Disabilities We know that fully supporting our caregivers is what creates the best outcomes for our patients. Our outstanding, comprehensive offerings are an investment in your health, well-being and future. What began in Cleveland in 1921 has grown to include locations throughout, the U.S. and even other countries. For you, that means more opportunities to learn, grow and serve patients — while finding caring, thriving communities both at work and at home. Cleveland Clinic is a nonprofit multispecialty academic medical center that integrates clinical and hospital care with research and education. Headquartered in Cleveland, Ohio, it was founded in 1921 by four renowned physicians with a vision of providing outstanding patient care based upon the principles of cooperation, compassion and innovation. Cleveland Clinic has pioneered many medical breakthroughs, including coronary artery bypass surgery and the first face transplant in the United States. U.S. News & World Report consistently names Cleveland Clinic as one of the nation’s best hospitals in its annual “America’s Best Hospitals” survey. Among Cleveland Clinic’s 70,800 employees worldwide represent 140 medical specialties and subspecialties. Cleveland Clinic is a 6,500-bed health system that includes a 173-acre main campus near downtown Cleveland, 19 hospitals, more than 220 outpatient facilities, and locations in southeast Florida; Las Vegas, Nevada; Toronto, Canada; Abu Dhabi, UAE; and London, England.

Responsibilities

The Research Coordinator III supports clinical trials across multiple ophthalmology subspecialties and collaborates closely with physicians and sponsors. Responsibilities include screening and enrolling patients, maintaining regulatory compliance, and managing investigational trials.