Director, Medical Information, Content & Review

🔥 2 minutes ago

🇺🇸 United States – Remote

⏰ Full Time

🔴 Lead

👨‍⚕️ Medical Director

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ADC Therapeutics

WebsiteLinkedInAll Job Openings

201 - 500 employees

🧬 Biotechnology

🏥 Healthcare

💊 Pharmaceuticals

Biotechnology • Healthcare • Pharmaceuticals

ADC Therapeutics is a commercial-stage global pioneer in the field of antibody drug conjugates (ADCs). The company focuses on transforming the lives of those impacted by cancer through a robust ADC portfolio targeting hematology and solid tumors. Their capabilities include a validated technology platform and a growing research & development toolbox, resulting in an approved product, ZYNLONTA®, for treating diffuse large B-cell lymphoma. Founded in 2011 and based in Lausanne, Switzerland, with operations in London and New Jersey, ADC Therapeutics is committed to confronting cancer and advancing treatment paradigms.

📋 Description

• Lead the Medical Information function and provide strategic leadership across Medical Affairs content development, medical review, and scientific training • Develop Medical Information strategy, inquiry management processes, scientific response content, literature surveillance, policies, quality standards, metrics, and continuous improvement initiatives • Oversee Medical Information resources such as standard response letters and other scientific response materials • Provide strategic and operational oversight of the outsourced Medical Information contact center, including vendor onboarding, training, budget, service levels, KPIs, quality, customer experience, compliance, and audit readiness • Lead or oversee Medical Affairs resources, including Field Medical resources, scientific decks, congress materials, training materials, and medical website/digital content • Ensure scientifically accurate, balanced, compliant responses to unsolicited and off-label requests • Own medical review of non-promotional materials and represent Medical Affairs in promotional material review • Partner with Legal, Regulatory, Compliance, Commercial, Medical, Clinical Development, Drug Safety/Pharmacovigilance, Market Access, and other stakeholders on content review and scientific communications • Ensure adverse events, product complaints, and safety-relevant information are identified, documented, and routed within required timelines • Develop and support Medical Affairs scientific training, onboarding, disease-state, product, pipeline, and clinical-data training • Monitor compendia, clinical guidelines, and clinical pathways and lead related submission and communication activities with Market Access • Analyze Medical Information inquiries and customer interactions to identify trends, knowledge gaps, and actionable insights • Maintain current knowledge of scientific literature, treatment guidelines, therapeutic-area developments, competitive data, and internal clinical data • Provide Medical Information, content, review, and training support for product launches, new indications, clinical data releases, congresses, and scientific milestones • Develop and maintain Medical Information and content-related policies, SOPs, work instructions, and governance processes • Manage external vendors and associated budgets • Perform other duties as assigned

🎯 Requirements

• PharmD, PhD, MD, or other relevant advanced scientific or clinical degree required • Minimum of 8 years of relevant pharmaceutical or biotechnology industry experience, including significant experience in Medical Information • Demonstrated experience developing and maintaining Medical Information content, including scientific response materials • Demonstrated experience in Medical Affairs content development and translating complex scientific and clinical information into clear, accurate, audience-appropriate scientific communications • Experience performing medical/scientific review of non-promotional materials and representing Medical Affairs in promotional review processes • Strong understanding of Medical Information requirements, scientific communication principles, pharmaceutical industry standards, and applicable regulatory and compliance considerations • Demonstrated ability to independently lead complex initiatives and functional responsibilities within a cross-functional, matrixed organization • Working knowledge of U.S. requirements for unsolicited requests, adverse event and product complaint reporting, and promotional review • Strong scientific acumen and ability to critically evaluate clinical data, scientific literature, treatment guidelines, and other medical evidence • Excellent written and verbal communication skills, with ability to communicate complex scientific concepts clearly and accurately to scientific and non-scientific audiences • Strong project management, prioritization, problem-solving, and decision-making skills • Ability to manage multiple priorities in a fast-paced biotechnology environment • Ability to build effective relationships and influence cross-functional stakeholders without direct authority • Hematology/oncology experience strongly preferred • Experience developing or delivering Medical Affairs scientific training and onboarding programs preferred • Experience managing outsourced Medical Information contact centers and/or other external Medical Affairs vendors preferred • Product launch and major clinical data-release experience preferred • Experience with compendia, clinical guideline, and/or clinical pathway submissions preferred • Experience managing vendors and budgets preferred • Travel requirements: <10% travel

🏖️ Benefits

• Competitive biotech base salary • Annual target bonus (eligibility based on company performance) • New hire stock options • Medical, Dental and Vision benefits starting on the 1st day of employment • 401(k) with company match • Paid time off and company holidays, including a company-wide shutdown at the end of the year • Paid Parental Leave • Life and Disability Insurance • Tax-advantaged health savings and spending accounts • Hands-on, collaborative culture • Mission-driven work that puts patients first

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