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QARA

Deegit

Plymouth, MN, us

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About the role

Additional Information

All your information will be kept confidential according to EEO guidelines.

Company Description

Deegit Inc.

Job Description

Job Description:

  • The Clinical Subject Matter Expert (SME) will be responsible for the clinical support of device risk management activities.
  • SME will have the following responsibilities:
  • Review and approval of the clinical workflow definitions for the subject devices
  • Identification of the clinical hazards and associated harms for the subject devices
  • Estimation of the severity and probability of occurrence for the clinically related hazardous situation
  • Development of the clinical benefit statements for the subject device

Key skills and experience:

  • A degree in a clinical related field (RN, MD)
  • 10 years of clinical experience

Additional skills (Desirable)

  • Understanding of device development in an FDA regulated environment
  • Experience with ISO 14971 risk management activities
  • Experience with the post market medical device support (complaint or risk analysis)

Skill and Experience Details:

Minimum Experience Required:

Mandatory Skills: Medical Data Acquisition and Storage Consulting

Desirable Skills: Clinical Systems, Medical Devices - QARA Language Skills: English Language