Senior Medical Writing Associate
Posted 2026-05-05
Remote, USA
Full-time
Immediate Start
- 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