Senior Medical Writing Associate

Job Description: • Serve as medical writing contributor or lead for clinical trial-related regulatory documents • Write/edit/review content of clinical trial-associated documents for new and ongoing programs • Work with cross-functional teams to ensure production of high-quality written documents • Perform literature searches as needed and summarize data for incorporation into documents • Adhere to company Style Guide, templates, and SOPs for document development • Commit to company timelines for all assigned documents Requirements: • Bachelor’s degree required; advanced degree in life sciences preferred • BA/BS and 6+ years of relevant experience (less with advanced degree) • Strong scientific background in cellular immunology or related field, or oncology, is a plus • Experience with generating text from data or literature • Experience with clinical trial-related report documents is a plus • Demonstrated advanced writing skills with strong command of English language and grammar • Proficiency with MS Office Suite, EndNote, and MS Word templates • Strong oral and written communication skills • Efficient, organized, and able to handle short timelines in a fast-paced environment • Ability to work both independently and collaboratively • Ability to identify issues, ask questions, and propose solutions Benefits: • company-sponsored medical, dental, vision, and life insurance plans* • discretionary annual bonus • discretionary stock-based long-term incentives (eligibility may vary based on role) • paid time off