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Research Coordinator II

4 months ago


Cleveland, United States Cleveland Clinic Full time

Join the Cleveland Clinic team, where you will work alongside passionate caregivers and provide patient-first healthcare. Cleveland Clinic is a top ranked hospital in the United States. 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's Main Campus is looking to add a Research Coordinator to their Institute. You will be joining a multi-disciplinary, talented team that works on studies that impact future patient diagnoses and treatments. As a Research Coordinator, you will coordinate the compliant implementation and conduct of human subject research projects, typically of medium workload and medium complexity. The future caregiver is someone who: -Has research and clinical experience. -Has experience working in EPIC and with spreadsheets. -Excels working independently and as part of a team. -Is organized and detail-oriented. This opportunity allows you to be valued as a team member and supported as you achieve your goals. You will have opportunities for learning, career growth, and professional development. Cleveland Clinic provides what matters most: career growth, delivering world-class care to our patients, continuous learning, exceptional benefits and working for an organization that offers many long-term career paths. Join us and experience a culture where opportunities to advance and the support to get there go hand-in-hand.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 pletes 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 externalconstituents.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:High School Diploma or GED. Associate's or Bachelor's degree in health care or science related field preferred.Bachelor's degree in healthcare or science field may offset two years of 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.Continually demonstrates competency with defined requirements for the position as established by Cleveland Clinic. Education preference.Certifications:None plexity 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.Preferred Qualifications: 3 years of clinical research experiencePhysical Requirements:Ability to perform work in a stationary position for extended periodsAbility to operate a computer and other office equipmentAbility to communicate and exchange accurate informationIn some locations, ability to move up to 25 poundsPersonal Protective Equipment:Follows standard precautions using personal protective equipment as required. Pediatric Neurology Neuromuscular Research Coordinator, Research Neuro, Research Associate Peds NeuroPay RangeMinimum hourly: $20.77Maximum hourly: $31.68The 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.