Senior Medical Documentation Specialist

3 days ago


madurai, India beBeeRegulatory Full time

As a Regulatory Medical Writer, you will be responsible for creating and revising regulatory documents, including those related to clinical trials and product approvals.This role requires strong writing skills, attention to detail, and the ability to interpret complex scientific data. You will work closely with cross-functional teams to ensure that all documentation meets the highest standards of quality and accuracy.Key responsibilities include drafting and editing documents, conducting literature reviews, and collaborating with colleagues to achieve shared goals.A strong understanding of regulatory guidelines, medical terminology, and scientific principles is essential for success in this role.Proficiency in Microsoft Office Suite, particularly Word, Excel, and PowerPoint, is also required.In addition, you will need excellent organizational and communication skills, as well as the ability to meet tight deadlines and prioritize multiple tasks effectively.



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