Senior Medical Content Specialist

23 hours ago


Jodhpur, India beBeeContentCreation Full time

About the Role:We are seeking a skilled Medical Writer to join our team.Key Responsibilities:Create, update, and manage regulatory documents including Clinical Evaluation Reports, Summary of Safety and Clinical Performance Reports, State of the Art Reviews, and Systematic Literature Reviews.Write and update CERs, SSCPs, SOAs, and LRRs in compliance with applicable regulatory requirements and guidelines.Participate in systematic literature reviews, including search, screening, data extraction, analysis, and synthesis.Summarize clinical, non-clinical, and regulatory data for risk/benefit analyses on medical devices.Compare device safety and performance against the state of the art and investigate unexpected outcomes.Utilize software systems like Microsoft Office, EndNote, Distiller, Wrike, and AI tools to create required documents.Requirements:Demonstrated experience in medical writing and document management.Strong understanding of regulatory requirements and guidelines.Excellent communication and analytical skills.Ability to work independently and as part of a team.Benefits:Ongoing training and professional development opportunities.A dynamic and supportive work environment.The chance to work on challenging projects and make a meaningful contribution.



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