Job Description
This description is a summary of our understanding of the job description. Click on 'Apply' button to find out more. Role Description This role involves the development, coordination, and execution of high-quality scientific publications, congress materials, and medical content that communicate clinical and translational data accurately, compliantly, and effectively. • Support the development and execution of the global medical communication and publication plans aligned with Medical Affairs and clinical program objectives • Author, edit, and manage a range of publication and other medical communication deliverables, including: • Primary manuscripts • Review articles • Abstracts • Slide Decks (MSL and HCP) • Congress posters and oral presentations • Plain language summaries (as applicable) • Ensure content is scientifically accurate, balanced, and aligned with source data • Translate complex clinical, preclinical, and translational data into clear, compelling scientific narratives • Manage internal review, approval workflows, and version control • Partner with Clinical Development, Biostatistics, Regulatory, Commercial (as appropriate), and external medical writers • Support author engagement, including coordinating feedback and revisions with key opinion leaders (KOLs) • Inquiry management – Monitor the inquiry inbox and respond to patient and physician inquiries using approved templates Qualifications • Advanced degree in a scientific or medical discipline (PhD, PharmD, MD, or MS with relevant experience) • 10+ years of medical or scientific writing experience in publications within biotech, pharma, or medical communications • Demonstrated experience authoring manuscripts, abstracts, and congress materials • Strong understanding of clinical trial design, statistics, and data interpretation • Working knowledge of publication ethics and guidelines (ICMJE, GPP) • Experience supporting publications for cell therapy, immunology, or rare/autoimmune diseases • Exceptional scientific writing and editing skills • Strong project management and organizational abilities • Ability to work independently while collaborating effectively across functions • High attention to detail and commitment to quality and compliance • Clear communicator with the ability to manage competing priorities Requirements • Hourly rate: $90/hr-$110/hr • Duration: 12 months, 15-30 hours per week depending on workload Apply tot his job