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Clinical Research Associate I or II, Cleveland, OH

Primary Responsibilities

  • Coordinates and implements clinical study activities for product development projects.
  • Works directly with the clinical, research, and regulatory staff to execute clinical studies.
  • Trains clinical site staff on study protocols, good clinical practices and use of investigational devices.
  • Coordinates and monitors clinical studies to ensure compliance with study protocols, regulatory requirements and Good Clinical Practices.


  • BS degree or higher in Life Sciences or related technical or clinical field.
  • 1-2 years related research and monitoring experience preferred, preferably in the Medical Device industry.
  • Experience with the design, management and conduct of medical device or drug related clinical studies.
  • Knowledge of FDA guidelines and Good Clinical Practices.
  • Ability to travel up to 20% depending on the clinical studies.

Why Join Our Team?

  • Excellent career opportunity in a rewarding medical device industry
  • Small, collaborative office environment
  • Competitive compensation and benefits
  • Employee Wellness Program
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