Cleveland Clinic - Cleveland, OH

posted 3 months ago

Full-time - Entry Level
Remote - Cleveland, OH
1,001-5,000 employees
Ambulatory Health Care Services

About the position

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. In this role as a Research Coordinator I, 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 coordinating the implementation and conduction of research projects, communicating with sponsors, monitors, and research personnel to ensure all aspects of study compliance, and assisting in the development and maintenance of research tools. The ideal caregiver is someone who is detail-oriented, works with integrity and transparency, is a respectful team player that can also work independently, and is organized and can prioritize to meet deadlines. You will work in a dynamic and technologically advanced environment that allows you to discover, learn, and grow across different institutes and locations. You'll be completely supported professionally and personally by our department, who genuinely cares about your well-being. This role is also hybrid, allowing you to work from home 2 days a week once your training is completed. 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.
  • Communicates with sponsors, monitors, and 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.
  • Monitors and reports project status and completes regulatory documents, data capture, and monitoring plans.
  • Assists with completion of protocol-related activities and may be required to attain and maintain clinical competencies for unlicensed caregivers.
  • Maintains study personnel certification records and documents the education and training of research personnel as needed.
  • May participate in the conduct and documentation of the informed consent process and contribute to research project budget development.

Requirements

  • High School Diploma or GED required; Associate or bachelor's degree in health care or science related field preferred.
  • Minimum two years clinical research or healthcare experience required; 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.
  • Solid written and verbal communication skills; must be self-directed with demonstrated ability to work in collaboration with 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.

Nice-to-haves

  • Experience in clinical research or healthcare settings.
  • Familiarity with regulatory documents and IRB submissions.
  • Knowledge of Good Clinical Practice (GCP) guidelines.

Benefits

  • Dental insurance
  • Health insurance
  • Vision insurance
  • Work from home options
  • Comprehensive benefits package including healthcare/dental/vision and retirement options.
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