Cleveland Clinic - Cleveland, OH

posted 2 months ago

Full-time
Cleveland, OH
Ambulatory Health Care Services

About the position

Join Cleveland Clinic's Taussig Cancer Center and become part of one of the most respected healthcare organizations in the world. Known for its continuous clinical trials and cancer research, the Taussig Cancer Center ensures all patients receive top-quality patient care and have access to the newest advances in cancer treatment. As a Clinical Research Coordinator, you will coordinate the compliant implementation and conduct of human subject research projects. You will work in a dynamic and technologically advanced environment that allows you to discover, learn and grow. You'll remain professionally challenged as you shape the career of your dreams and find where you belong, here at Cleveland Clinic. A caregiver in this position works days, with hours typically scheduled between 7 a.m. - 4:30 p.m. This is a PRN position. Start and end times and total hours worked weekly may vary. A caregiver who excels in this role will assist with the coordination, implementation, and conduct of research projects ensuring adherence to research protocol requirements. You will communicate with sponsors, monitors, and research personnel to ensure all aspects of study compliance. Collaboration with the study team to schedule pre-site selection visits, site initiation visits, webinars, monitoring, and close-out visits is essential. You will also monitor and report on project status, complete regulatory documents, data capture, and monitoring plans, and monitor research data to maintain quality.

Responsibilities

  • Assist with the coordination, implementation, and conduct of research projects ensuring adherence to research protocol requirements.
  • Communicate with sponsors, monitors, and research personnel to ensure all aspects of study compliance.
  • Collaborate with the study team to schedule pre-site selection visits, site initiation visits, webinars, monitoring, and close-out visits.
  • Monitor and report on project status.
  • Complete regulatory documents, data capture, and monitoring plans.
  • Monitor research data to maintain quality.

Requirements

  • High school diploma or GED.
  • Minimum two years clinical research or healthcare experience required.
  • Demonstrated proficiency with computer-based word processing, spreadsheet, and presentation software.

Nice-to-haves

  • Associate or bachelor's degree in healthcare or science field may offset experience requirement.
  • Bachelor's degree in a health care or science related field.

Benefits

  • Healthcare insurance
  • Dental insurance
  • Vision insurance
  • Retirement plan
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