Research Coordinator I - Neurology

at  Cleveland Clinic

Join Cleveland Clinic’s Neurology Division where research and surgery are advanced, technology is leading-edge, patient care is world-class, and caregivers are family. Cleveland Clinic is recognized as one of the top hospitals in the country. 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.
As a Research Coordinator I, you will demonstrate exceptional coordination and compliance of the implementation and conduct of human subject research projects, typically of low workload and low complexity. You will also assist with research study design and protocol development.

The ideal future caregiver is someone who:

• Has clinical research experience
• Is flexible and self-motivated.
• Pays close attention to detail.
• Thrives working independently and as part of a team.

By taking this opportunity, you will join an inclusive, supportive team that strongly believes in supporting one another in both personal and career goals and promoting from within the team. This position is located at Cleveland Clinic Las Vegas. Candidate must be able to work onsite.

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

• Coordinate the compliant implementation and conduct of human subject research projects typically of medium workload and medium complexity.
• Maintain regulatory documents and binders, data management, IRB submissions and communications.
• Report and complete Serious Adverse Events and/or safety logs as defined per protocol as they occur.
• Complete Food and Drug Administration (FDA) and sponsor forms in accordance with GCP guidelines.
• Communicate with sponsors, monitors, 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 the study team to schedule pre-site selection visits, site initiation visits, webinars, monitoring and close-out visits.
• Collaborate with the primary investigator, sponsor and research staff to plan, conduct and evaluate project protocols, including research subject recruitment.
• Monitor and report project status.
• Completes regulatory documents, data capture, monitoring plans and protocol-related activities.
• Attain and maintain clinical competencies for unlicensed caregivers such as phlebotomy, vital signs, ECG, POC testing and other testing as required.
• Monitor research data to maintain quality.
• Demonstrate comprehension of assigned research protocols.
• Develop and maintain knowledge of research protocols to coordinate the comprehensive and compliant execution of assigned protocols.
• Assist with preparing audits and responses to audits.
• Assist in the development and maintenance of research tools, such as spreadsheets, questionnaires and/or brochures.
• Maintain study personnel certification records (License, CV, CITI).
• Document the education and training of research personnel as needed.
• Participate in the conduct and documentation of the informed consent process.
• Assist the PI with research study design and developing research protocol