Document Specialist

6 days ago


rajkot, India beBeeMedical Full time

Medical Document SpecialistA meticulous professional will create, update and manage regulatory documents within the medical device industry.Create and maintain Clinical Evaluation Reports (CERs), Summary of Safety and Clinical Performance Reports (SSCPs) in compliance with applicable regulatory requirements.Conduct systematic literature reviews including search, screening, data extraction, analysis and synthesis to support clinical documentation.Analyze and summarize clinical and non-clinical data for risk/benefit assessments on medical devices.Responsibilities:Development of high-quality clinical documents.Literature review and analysis.Data interpretation and summarization.Requirements:Strong research skills and attention to detail.Excellent communication and analytical skills.Familiarity with regulatory requirements.Benefits:Opportunity to work with a dynamic team.Professional growth and development.Competitive compensation package.We Offer:A collaborative work environment.Ongoing training and education.A comprehensive benefits package.



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