Report writer serp_jobs.h1.location_city

A company is looking for a Medical Writer responsible for developing and managing medical writing deliverables to support clinical regulatory writing. Key Responsibilities Develop strategies and manage projects for regulatory submissions and clinical deliverables Coordinate and author regulatory documents, ensuring integration of scientific, medical, and regulatory input Produce high-quality documentation in line with regulatory / compliance / scientific requirements Required Qualifications, Training, and Education 10+ years of experience in the research, medical, pharmaceutical, or biotechnology industry Minimum of 8+ years of experience as a medical writer in the pharmaceutical and / or biotech industry, focusing on oncology or rare diseases Bachelor's Degree required; Advanced Degree preferred Technical expertise in Microsoft Office, Adobe Acrobat, and familiarity with document management systems Good understanding of global pharmaceutical drug development and regulatory submission requirements