Regulatory Specialist

2 weeks ago


junagadh, India beBeeMedicalWriter Full time

Regulatory and Clinical Document ProfessionalsCreate, update and manage regulatory and clinical documents in the medical device sector.Key Responsibilities:Develop and maintain high-quality Clinical Evaluation Reports, Summary of Safety and Clinical Performance Reports, State of the Art Reviews, and Systematic Literature Reviews.Participate in systematic literature reviews, including search, screening, data extraction, analysis, and synthesis.Analyze and summarize clinical, non-clinical, and regulatory data to inform risk/benefit analyses on medical devices.Required Qualifications:Bachelor's degree in a life science or related field.Minimum three years' experience in medical writing or a related role.Benefits:Opportunity to contribute to the development of critical regulatory and clinical documentation for the medical device sector.



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