Principal Research Technologist

Cleveland Clinic
•Onsite

About The Position

At Cleveland Clinic Health System, we believe in a better future for healthcare. And each of us is responsible for honoring our commitment to excellence, pushing the boundaries and transforming the patient experience, every day. We all have the power to help, heal and change lives — beginning with our own. That’s the power of the Cleveland Clinic Health System team, and The Power of Every One.

Requirements

  • Master's Degree in Biological Sciences or a Bachelor's Degree plus 15 years of independent research, which includes the ability to perform independent research projects.
  • Demonstrated and thorough understanding of research techniques, procedures, protocols and management of the laboratory are essential.
  • Ability to direct the work of others.
  • A minimum of ten years of related experience in a research laboratory.
  • 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.
  • 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
  • Ability to distinguish color
  • Manual dexterity to handle specimens and repair equipment
  • Ability to lift and transport equipment or specimens weighing up to 20 pounds
  • May be exposed to hazardous chemicals, bio-hazards, radioactive materials, etc.
  • Follows standard precautions using personal protective equipment as required.

Nice To Haves

  • Ph.D. Degree may substitute for some experience.

Responsibilities

  • Plans, organizes, performs and monitors daily project protocols.
  • Collects, prepares and maintains required research documentation, including informed consent records, case records, clinical notes and medical reports.
  • Assists the Principal Investigator in constructing and submitting grant proposals.
  • Reports and assists with the management of protocol deviations, adverse events and other project-related issues.
  • Safeguards the use of drugs and maintains legal requirements for experimental drug usage as needed.
  • Assists with the preparation and delivery of internal/external presentations, conference reports/lectures, and publishing submissions.
  • Other duties as assigned.

Benefits

  • Drug free environment
  • Influenza prevention program (annual vaccination or approved exemption)
  • Equal employment opportunity
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