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Join the Cleveland Clinic team, where you will work alongside passionate caregivers and provide patient-first healthcare. Cleveland Clinic is recognized as one of the top hospitals in the nation. 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.Cleveland Clinic is looking to add a Research Coordinator II to their dedicated team of caregivers. As a Research Coordinator II, you will directly facilitate clinical research that allows Cleveland Clinic to continue to innovate and drive better outcomes and healthcare for patients. Your duties will include but are not limited to:Coordinating the implementation and conduction of research projects.Communicating with sponsors, monitors, and research personnel to ensure all aspects of study compliance.Assisting in the development and maintenance of research tools.The ideal caregiver is someone who:Is detailed-oriented.Has at least 3 years of research experience.Is a respectful team-player that can also work independently.Is organized and can prioritize, making sure to meet deadlines.As a Research Coordinator II, you will work in a dynamic and technologically advanced environment that allows you to discover, learn, and grow across different institutes and locations.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:
Coordinates the implementation and conduct of research projects ensuring adherence to research protocol requirements including: timely completion and communication of regulatory documents, the development of data capture and monitoring plans, reporting of Serious Adverse Events as they occur and completion of Food and Drug Administration (FDA) and sponsor forms in accordance with GCP timelines.
Serves as a liaison between investigators, research personnel, outside study personnel and central research administration offices to assist in protocol interpretation, enrollment and safety questions.
Collaborates 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.
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.
Maintains professional relationships, including frequent and open effective communication with internal and external
constituents.
Assists with the development of training and educational material for assigned research protocols.
Provides and documents education as needed.
Conducts and documents the informed consent process.
Potentially assists with research project budget development.
Other duties as assigned.
Education:
Bachelor's degree in health care or science related field preferred.
Bachelor's degree in healthcare or science field may offset two years of clinical research experience requirement.
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.
Continually demonstrates competency with defined requirements for the position as established by Cleveland Clinic.
Demonstrated basic computer proficiency.
Strong organizational, communication and interpersonal skills.
Must be self-directed with demonstrated ability to work independently yet establish cooperative relationships with colleagues.
Certifications:
None required.
Complexity of Work:
Requires critical thinking skills, decisive judgment and the ability to work with minimal supervision.
Must be able to work in a stressful environment and take appropriate action.
Work Experience:
Minimum three years clinical research experience required.
Bachelor's degree in healthcare or science field may offset two years of clinical research experience requirement.
Physical Requirements:
A high degree of dexterity to produce materials on a computer.
Requires normal or corrected vision and hearing to normal range.
Extensive sitting and frequent walking, occasional lifting or carrying up to 25 pounds.
May have some exposure to communicable diseases or body fluids.
May require working irregular hours.
Personal Protective Equipment:
Follows standard precautions using personal protective equipment as required.
Pay RangeMinimum hourly: $22.85Maximum hourly: $34.85The 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
Full-time