Job Description

Join to apply for the Senior Medical Writer role at ImmunityBio, Inc. 6 days ago Be among the first 25 applicants Join to apply for the Senior Medical Writer role at ImmunityBio, Inc. Company Overview ImmunityBio, Inc. (NASDAQ: IBRX) is a commercial-stage biotechnology company developing cell and immunotherapy products that are designed to help strengthen each patient’s natural immune system, potentially enabling it to outsmart the disease and eliminate cancerous or infected cells. We envision a day when we no longer fear cancer, but can conquer it, thanks to the biological wonder that is the human immune system. Our scientists are working to develop novel therapies that harness that inherent power by amplifying both branches of the immune system, attacking cancerous or infected cells today while building immunological memory for tomorrow. The goal: to reprogram the patient’s immune system and treat the host rather than just the disease. Why ImmunityBio? Developing cutting-edge technology to transform the lives of patients with cancer and infectious diseases. Opportunity to join a publicly traded biopharmaceutical company based in Southern California. Collaborative work environment across different areas of the company. Growing company with professional development opportunities. Position Summary The Senior Medical Writer will prepare high-quality regulatory documents such as clinical study reports, summaries, protocols, Investigator’s brochures, and informed consent forms. They will handle complex writing assignments and serve as a subject matter expert. They may also manage internal and external communications of scientific and clinical data, including abstracts, presentations, manuscripts, and educational materials. Essential Functions Lead complex medical writing projects, collaborating with cross-functional teams. Serve as a subject matter expert in assigned therapeutic areas. Mentor less experienced writers. Resolve issues in the writing process, escalating when necessary. Draft and finalize clinical and regulatory documents. Write for diverse audiences, including scientists, physicians, regulators, and patients. Collaborate with other teams to gather source data and prepare documents. Lead review meetings and provide content direction. Perform quality control of documents. Ensure documents meet eCTD formatting and hyperlinking standards. Education & Experience Bachelor’s degree in a science-related field with 4+ years of relevant experience, or Master’s degree with 2+ years of relevant experience. Experience with NDA submissions, CSRs, IBs, and clinical protocols. Strong background in oncology, immunotherapy, or related fields. Knowledge, Skills, & Abilities Proficiency in AMA guidelines and FDA, EMA, ICH regulations. Excellent communication skills in English. Understanding of drug development and clinical data interpretation. Strong project management and attention to detail. Proficiency in MS Office, Adobe Acrobat, EndNote, and eCTD tools. Working Environment Onsite position with standard office environment. Work schedule: Monday – Friday, with flexibility. Ability to lift up to 20 pounds. This role offers a discretionary bonus and equity, with a salary range of $117,000 to $130,000 based on experience and location. #J-18808-Ljbffr ImmunityBio, Inc.

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