Job Details

A company is looking for a Consultant I, Medical Writing.Key ResponsibilitiesAuthor regulatory documents including Clinical Study Reports and submission materialsLead the development of complex regulatory modules and ensure document accuracyCoordinate regulatory projects and maintain strong client relationshipsQualifications and RequirementsAdvanced degree in a life or health science discipline preferredStrong foundation in medical and regulatory writingExceptional project and time management skillsProficiency in Microsoft Office Suite and familiarity with regulatory document management systemsExperience with regulatory submissions and understanding of global regulatory standards