Senior Document Specialist

7 days ago

erode, India beBeeRegulatoryMedicalWriter Full time

Job TitleA Regulatory Medical Writer is a vital role in the clinical research industry.This position involves drafting, reviewing, and finalizing regulatory documents such as clinical study reports, investigator brochures, and other essential documents.The individual in this role will be responsible for performing literature reviews, adhering to regulatory guidelines, collaborating with cross-functional teams, and ensuring the accuracy and quality of scientific communication.ResponsibilitiesDrafting and finalizing regulatory documents including clinical study reports and investigator brochures.Performing literature reviews and ensuring adherence to regulatory guidelines.Collaborating with cross-functional teams to ensure successful outcomes.Ensuring the accuracy and quality of scientific communication.About This RoleThis is an excellent opportunity for a detail-oriented and organized individual to work in a fast-paced environment.The ideal candidate will have strong analytical skills, attention to detail, and the ability to work effectively in a team.RequirementsBachelor's degree in a life science or related field.Experience in medical writing or a related field.Strong knowledge of regulatory guidelines and industry standards.Excellent communication and interpersonal skills.

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