• Provide high-quality medical and scientific writing from planning and coordination through delivery of final drafts • Collaborate with internal and external clients • Support and enable effective and efficient communication resulting in operational excellence • Author clinical and preclinical regulatory documents with expertise in infectious diseases and/or oncology • Serve as a primary author for clinical documents • Review routine documents prepared by team members • May provide training and mentorship for writers • Ensure compliance with quality processes and requirements • Develop best practices, methods, and techniques for achieving optimal results