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. At Cleveland Clinic, you will work alongside passionate and dedicated caregivers, receive endless support and appreciation, and build a rewarding career with one of the most respected healthcare organizations in the world.

　　This position directly facilitates clinical research that allows Cleveland Clinic to continue to innovate and drive better outcomes and healthcare for patients. As a Research Coordinator, you will coordinate the compliant implementation and conduct of human subject research projects. You will work closely with other Research Coordinators, Research Nurses and Clinical Project Managers and will report to the Research Program Manager. We all work as a team and are respectful and supportive of one another.

　　The ideal caregiver is someone who:

　　Thrives in a team environment.

　　Is organized and detail-oriented.

　　Demonstrates a strong work ethic and communication skills.

　　Has strong and confident coordination skills.

　　Is a team-player who can also work independently.

　　As a Research Coordinator, you will work in a dynamic and technologically advanced environment that allows you to discover, learn and grow. There are many opportunities for professional development and advancement within our team. We support many different types of clinical trials and work with many institutes across Cleveland Clinic. This increases a Caregiver's exposure to the enterprise and affords many networking, career development and advancement opportunities.

　　At Cleveland Clinic, we know what matters most. That's why we treat our caregivers as if they are our own family, and we are always creating ways to be there for you. Here, you'll find that we offer: resources to learn and grow, a fulfilling career for everyone, and comprehensive benefits that invest in your health, your physical and mental well-being and your future. When you join Cleveland Clinic, you'll be part of a supportive caregiver family that will be united in shared values and purpose to fulfill our promise of being the best place to receive care and the best place to work in healthcare.

　　Responsibilities:

　　Assists with the coordination, implementation, and conduct of research projects ensuring adherence to research protocol requirements which may include: maintenance of regulatory documents and binders, data management, IRB submissions and communication of such to the research team.

　　May be responsible for reporting/completion of Serious Adverse Events and/or safety log as defined per protocol as they occur and completion of Food and Drug Administration (FDA) and sponsor forms in accordance with GCP guidelines as applicable.

　　Communicates with sponsors, monitors, research personnel to ensure all aspects of study compliance.

　　Collaborates with study team to schedule pre-site selection visits, site initiation visits, webinars, monitoring and close-out visits.

　　May collaborate with primary investigator, sponsor and research staff to plan, conduct and evaluate project protocols, including research subject recruitment.

　　Monitors and reports project status.

　　Completes regulatory documents, data capture and monitoring plans.

　　Assists with completion of protocol related activities.

　　As delegated, may be required to attain and maintain clinical competencies for unlicensed caregivers such as phlebotomy, vital signs, ECG, POC testing and other testing as required.

　　Monitors research data to maintain quality.

　　Understands basic concepts of study design.

　　Demonstrates comprehension of assigned research protocols.

　　Develops and maintains knowledge of research protocol to coordinate the comprehensive and compliant execution of assigned protocols.

　　Assists with preparation for audits and response to audits.

　　May assist in the development and maintenance of research tools, such as spreadsheets, questionnaires and/or brochures.

　　Maintains study personnel certification records (License, CV, CITI).

　　Maintains professional relationships, including frequent and open effective communication with internal and external customers.

　　Documents the education and training of research personnel as needed.

　　May participate in the conduct and documentation of the informed consent process.

　　May contribute to research project budget development.

　　Performs other duties as assigned.

　　Education:

　　High School Diploma or GED. Associate's or Bachelor's degree in health care or science related field preferred. Degree may offset experience requirement.

　　Demonstrated proficiency with a variety of computer-based skills, especially in the use of word processing spreadsheets, database and presentation software, and the ability to undertake internet searches.

　　Solid written and verbal communication skills.

　　Must be self-directed with demonstrated ability to work in collaboration and cooperation with members of a multidisciplinary team.

　　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.

　　Languages:

　　Language required

　　Language preferred

　　Certifications:

　　None required.Complexity of Work:

　　Requires excellent organizational, written, and verbal communication skills.

　　Must be able to take direction and appropriate action in a stressful environment.

　　Work Experience:

　　Minimum two years clinical research or healthcare experience required.

　　Associate's or Bachelor's degree in healthcare or science field may offset experience requirement.

　　Demonstrated proficiency with a variety of computer-based skills, especially in the use of word processing, spreadsheets, database and presentation software, and the ability to undertake internet searches. Solid written and verbal communication skills.

　　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.Pay Range

　　Minimum hourly: $20.77

　　Maximum hourly: $31.68

　　The pay range displayed on this job posting reflects the anticipated range for new hires. While the pay range is displayed as an hourly rate, Cleveland Clinic recruiters will clarify whether the compensation is hourly or salary. A successful candidate's actual compensation will be determined after taking factors into consideration such as the candidate's work history, experience, skill set, and education. This is not inclusive of the value of Cleveland Clinic's benefits package, which includes among other benefits, healthcare/dental/vision and retirement.

　　Cleveland Clinic Health System is pleased to be an equal employment employer: Women / Minorities / Veterans / Individuals with Disabilities