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