Onsite Medical Writer II – Clinical Evaluation Reporting, Medical Devices

Posted 3 weeks ago

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About the role

  • Medical Writer creating Clinical Evaluation Reporting documents for medical devices across multiple locations in the US. Involves technical and strategic writing expertise throughout product development and life cycle process.

Responsibilities

  • Writes and contributes to Clinical Evaluation reporting deliverables
  • Evaluates and summarizes clinical evidence
  • Analyzes results in preparation for product applications and submissions
  • Collaborates with team members and stakeholders in planning for and supporting CER related projects
  • Effectively communicates and collaborates with various departments

Requirements

  • Bachelor's degree in Science, Medical Technology, English OR an equivalent combination of education and work experience
  • Minimum 2 years relevant professional experience in R&D, Technical Product Development, Quality, Regulatory Affairs, Clinical Research, or Medical Writing
  • Comprehensive written and verbal communication skills
  • Strong organizational skills and attention to detail
  • Ability to critically review own work before sending out for internal/external review
  • Multitasking and prioritizing skills

Benefits

  • Career development with an international company
  • Free medical coverage in Health Investment Plan (HIP) PPO medical plan
  • Excellent retirement savings plan with high employer contribution
  • Tuition reimbursement
  • Freedom 2 Save student debt program and FreeU education benefit

Job title

Medical Writer II – Clinical Evaluation Reporting, Medical Devices

Job type

Experience level

JuniorMid level

Salary

$66,700 - $133,300 per year

Degree requirement

Bachelor's Degree

Location requirements

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