Sr Medical Writing Associate

Kite Pharma

1d•Onsite

About The Position

Kite is a biopharmaceutical company dedicated to curing cancer through the development of innovative cancer immunotherapies, specifically pioneering personalized CAR T-cell and T cell receptor (TCR) engineered cell therapies. The company's mission is to provide rapid, long-term durable responses and eliminate the burden of chronic care, empowering the immune system to recognize and kill tumors. Kite fosters a culture where every employee is valued, included, developed, and empowered, with People Leaders playing a crucial role in evolving this environment. The Senior Associate, Regulatory Writing is an individual contributor responsible for writing and/or editing clinical documents for various regulatory submissions, including INDs, BLAs, and MAAs, for new and ongoing programs. The company is based in Santa Monica, CA, and emphasizes curiosity, creativity, appreciation, and respect among its team members.

Requirements

Bachelor’s degree required
BA/BS and 6+ years of relevant experience (less with advanced degree)
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

Nice To Haves

Advanced degree in life sciences
Strong scientific background in cellular immunology or related field, or oncology
Experience with generating text from data or literature
Experience with clinical trial-related report documents

Responsibilities

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