Director, Medical Information, Content & Review in Fully

Transforming Cancer Therapy Together

At ADC Therapeutics, we are passionate about revolutionizing cancer treatment.

When you join our team, you become part of a mission-driven group of talented individuals dedicated to making a difference in patients' lives.

• Description
• Transforming Cancer Therapy Together

At ADC Therapeutics, we are passionate about revolutionizing cancer treatment.

When you join our team, you become part of a mission-driven group of talented individuals dedicated to making a difference in patients' lives.

Why ADC Therapeutics

ADC Therapeutics (NYSE): is a commercial, global leader and pioneer in the field of antibody-drug conjugates (ADCs) with specialized capabilities from clinical through commercialization.

Our CD-19-directed ADC for relapsed/refractory non-Hodgkin lymphoma, ZYNLONTA® (loncastuxamab tesirine lpyl) has received accelerated approval in the United States and conditional approval from the European Commission.

ZYNLONTA is also being evaluated in combination with other agents and in earlier lines of DLBCL therapy as well as in indolent lymphomas including follicular lymphoma and marginal zone lymphoma with the potential to reach significantly more patients through expanded use.

We are a team of approximately 150 patient-focused, purpose-driven employees with a shared mission to transform the treatment paradigm for patients.

If you’re interested in making a difference in the lives of patients worldwide with a team of like-minded colleagues, operating in a flexible work environment, come join us on our journey!

To learn more about ADC Therapeutics, our values, and our exceptional culture, please visit us at and Linked In.

Summary

The Director, Medical Information, Content & Review is an individual contributor responsible for leading the Medical Information function and providing strategic leadership across Medical Affairs content development, medical review, and scientific training.

This role ensures that accurate, current, balanced, and scientifically rigorous medical information is effectively developed and communicated to healthcare professionals, internal stakeholders, and other appropriate audiences.

The Director will have functional ownership of Medical Information strategy and operations, including medical inquiry management, development of scientific response content, literature surveillance, oversight of the outsourced Medical Information contact center, vendor and budget management, metrics and insights, and maintenance of compliant and audit-ready processes.

In addition, the role will represent Medical Affairs in the review of promotional materials and oversee the medical review of non-promotional materials to ensure medical accuracy, scientific integrity, and appropriate balance.

The Director will also work across medical affairs to develop and support scientific training, including onboarding and ongoing scientific training for Medical Affairs and Field Medical colleagues.

What You'll Do

• Medical

Information: Provide Medical Information strategy, inquiry management, scientific response content, literature surveillance, processes, policies, quality standards, metrics, insights, and continuous improvement.

• Scientific
• Response

Content: Oversee the development and maintenance of high-quality Medical Information resources, including standard response letters and other scientific response materials, ensuring content remains accurate, balanced, evidence-based, current, and compliant.

• Medical
• Information
• Contact

Center: Provide strategic and operational oversight of the outsourced Medical Information contact center, including vendor onboarding and ongoing disease-state, product, and escalation training, budget oversight, service-level agreements, KPIs, quality, customer experience, compliance, and audit readiness.

• Content

Development: Lead or oversee development of key Medical Affairs resources, including standard response letters, Field Medical resources, scientific decks, congress materials, training materials, and medical website/digital content.

• Unsolicited

Requests: Ensure all responses to unsolicited requests, including off-label inquiries, are scientifically accurate, balanced, and consistent with applicable regulations, guidance, and company policies.

Train internal colleagues on how to identify unsolicited requests and route them to Medical Information.

• Medical and
• Promotional

Review: Own the medical review of non-promotional materials and represent Medical Affairs in the review of promotional materials, providing scientific and medical expertise to support accuracy, currency, appropriate context, and fair and balanced presentation of data.

Partner with Legal, Regulatory, Compliance, Commercial, and Medical colleagues to establish and continuously improve efficient, consistent, and compliant content review processes.

• Adverse Event & Product
• Complaint

Handling: Ensure that adverse events, product quality complaints, and other safety-relevant information received through Medical Information channels, including the outsourced contact center, are identified, documented, and sent to Drug Safety/Pharmacovigilance and Quality within required timelines.

Partner with these functions on intake processes, reconciliation, vendor training, and audit and inspection readiness.

• Medical

Training: Work across medical affairs to develop and support Medical Affairs scientific training, including onboarding and ongoing disease-state, product, pipeline, and clinical-data training; support readiness for major data releases and congresses.

• Compendia, Guidelines & Pathways: Monitor the compendia, clinical guideline, and pathway landscape; identify appropriate opportunities for submissions or communications; and lead Medical Affairs activities related to compendia, guidelines, and clinical pathway submissions, in partnership with Market Access.
• Inquiry

Insights: Establish processes to monitor and analyze Medical Information inquiries and customer interactions, identify emerging questions, knowledge gaps, and trends, and communicate actionable insights to Medical Affairs leadership and relevant cross-functional stakeholders.

• Scientific

Expertise: Maintain current knowledge of relevant scientific literature, treatment guidelines, therapeutic-area developments, competitive data, and internal clinical data and apply this expertise across Medical Information, content, review, and training activities.

• Launch & Data-Release

Readiness: Provide strategic Medical Information, content, review, and training support for new product launches, new indications, major clinical data releases, congresses, and other significant scientific milestones.

• Governance & Compliance: Develop, maintain, and continuously evaluate Medical Information and content-related policies, SOPs, work instructions, and processes to ensure appropriate governance, quality, consistency, compliance, and inspection readiness.
• Cross-Functional

Partnership: Build strong working relationships across Medical Affairs and with Clinical Development, Drug Safety/Pharmacovigilance, Regulatory Affairs, Legal, Compliance, Commercial, Market Access, and other stakeholders to ensure coordinated scientific communication and effective execution of Medical Affairs priorities.

Actively partners with contact centers (Patient Support/Access) to ensure coordinated and efficient handling of inquiries.

• Vendor & Budget

Management: Manage external vendors and associated budgets within the role's areas of responsibility, ensuring appropriate scope, quality, performance, and stewardship of resources.

• Other duties, as assigned.

Requirements

Who You Are

• Pharm D, Ph D, 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 while operating effectively 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 with the ability to critically evaluate clinical data, scientific literature, treatment guidelines, and other sources of medical evidence.
• Excellent written and verbal communication skills, with demonstrated ability to communicate complex scientific concepts clearly and accurately to both scientific and non-scientific audiences.
• Strong project management, prioritization, problem-solving, and decision-making skills, with the ability to successfully manage multiple priorities in a fast-paced biotechnology environment.
• Demonstrated 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

What We Offer

• Competitive biotech base salary, annual target bonus (eligibility based on company performance) or quarterly IC (field sales roles) and new hire stock options – so you share in the value you help create
• Medical, Dental and Vision benefits which start on the 1st day of employment
• 401(k) with company match
• Paid time off and company holidays including a company wide shut down at the end of the year
• Paid Parental Leave, Life and Disability Insurance, Tax advantaged health savings and spending accounts
• A hands-on, collaborative culture with other passionate biotech professionals
• Mission-driven work that puts patients first
• Join Our Inclusive Team

ADC Therapeutics is an equal opportunity employer.

We are committed to building collaborative, engaged teams and fostering a professional and respectful work environment where employees are empowered for success.

We consider all qualified applicants without regard to any characteristic protected by law.

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