To support clinical research initiatives, the full-time remote Medical Writer will author clinical trial and regulatory documents, engage with cross-functional teams, and ensure document quality and compliance. Key responsibilities Author clinical trial and regulatory documents according to specified templates and guidelines Coordinate quality control processes for all documents produced Collaborate with cross-functional teams to develop clear and compliant documentation Required qualifications Master's degree with at least 5 years of medical writing experience in the Biotech/Pharmaceutical industry, or a Bachelor's degree with at least 8 years of relevant experience Proven ability to understand and interpret data for practical application Advanced knowledge of scientific and technical writing and editing Strong time and project management skills Experience in a collaborative team environment
Senior Project Engineer/Assistant Project Manager - Ground-Up Commercial ConstructionLocation: Phoenix, AZ (In-Office)Compensation: $90,000 - $125,000 base + bonus + full benefitsCompany: Top ENR-Ranked General ContractorAbout the CompanyWe are a well-established, highly...
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