Regulatory Affairs Specialist Job at LivaNova PLC, United States

  • LivaNova PLC
  • United States

Job Description

LivaNova PLC is seeking a Clinical Evaluation Writer for a remote position in the United States. The role involves preparing clinical evaluation plans and reports in line with EU MDR requirements, while managing the document workflow, and responding to regulatory queries.

To qualify, candidates should possess a master’s degree or Ph.D. in a relevant field, with significant experience in medical writing and regulatory affairs in the medical device sector. The estimated salary is between $85,000 and $95,000 plus a discretionary bonus.

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Job Tags

Remote work

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