Hiring: Associate Director, Medical Information, Oncology Company: Eisai US Location: Nutley, NJ Job Posted Time: 2026-09-16 13:48:13 Employment Type: Hybrid Target Skills & Keywords : Microsoft Office, Quality Assurance, Regulatory Compliance About the job Experience: •10+ years of experience in the pharma/biotech industry OR a combination of equivalent education and experience. Required Skills: •Develop and manage tactical execution of the Medical Information component of Global & US Medical Affairs strategic plans for assigned therapeutic area(s). •Develop and ensure high-quality, balanced, and scientifically accurate documents in response to medical inquiries from external customers and internal stakeholders; conduct quality assurance measures and handle escalated inquiries as needed. •Lead and drive the development of Medical Information deliverables, including research and analysis of the scientific literature, standard medical responses (SMRs), verbal responses to FAQs, AMCP dossiers, compendium and pathways submissions, etc. •Serve as medical reviewer, ensuring medical accuracy and provision of feedback for Eisai’s advertising, promotional, and medical materials as part of Copy Review Committee and Medical Review Committee. •Lead and provide oversight of department reporting processes, KPIs, insights analytics, digital analytics, and other trend reports that are shared with internal stakeholders; proactively identify opportunities to optimize insights for strategic decision-making. •Explore and implement AI-driven tools and technologies to enhance medical information processes, improve efficiency, and deliver innovative solutions for internal and external stakeholders. •Liaise with global and regional medical affairs colleagues as appropriate. •Provide strong scientific support for conference and booth coverage. Qualifications: •Advanced degree in sciences or related field with 10+ years of experience in the pharma/biotech industry OR a combination of equivalent education and experience. •Strong scientific knowledge and expertise in Oncology, including evaluating and communicating clinical trial and disease state information to a wide range of audiences. •Demonstrated experience in conducting scientific literature review, and management of medical inquiries, including the development and review of medical information deliverables (e.g., standard medical response documents, FAQs, dossier, compendium submissions, etc.) •Practical experience and knowledge of FDA guidance on appropriate scientific exchange practices. •Previous experience of managing/leading teams directly/indirectly or coaching and mentoring new hires/less experienced colleagues. •Proficiency with Microsoft Office Suite software, SharePoint, Veeva, customer relationship management software, and other technology and telephony systems. •Must be able to work hybrid in our Nutley, NJ office 3 days per week (Tuesday, Wednesday, Thursday) •Demonstrated capacity to identify and implement emerging technologies to optimize workflows and deliver innovative solutions. •In-depth knowledge of data visualization and insights reporting to support strategic decision-making. •The annual base salary range for the Associate Director, Medical Information, Oncology is from :$164,600-$216,100 Compensation: •$164,600 - $216,100 / year Interested candidates, please apply directly through the job posting on company's career page or try via AI auto apply on this platform. Don't miss this opportunity to join a forward-thinking team!