Director, Global Medical Affairs Strategy - Solid Tumors

Genmab•Princeton, FL

About The Position

At Genmab, we are dedicated to building extra[not]ordinary® futures, together, by developing antibody products and groundbreaking, knock-your-socks-off KYSO antibody medicines® that change lives and the future of cancer treatment and serious diseases. We strive to create, champion and maintain a global workplace where individuals’ unique contributions are valued and drive innovative solutions to meet the needs of our patients, care partners, families and employees. Our people are compassionate, candid, and purposeful, and our business is innovative and rooted in science. We believe that being proudly authentic and determined to be our best is essential to fulfilling our purpose. Yes, our work is incredibly serious and impactful, but we have big ambitions, bring a ton of care to pursuing them, and have a lot of fun while doing so. Does this inspire you and feel like a fit? Then we would love to have you join us! Director, Global Medical Affairs Strategy – Solid Tumors The Role: The Genmab pipeline comprises of robust and diverse antibody products in immuno-oncology and beyond. Reporting to the Global Medical Affairs Strategy Lead (MASL) the Director will be responsible for the development and execution of the Global Medical Affairs strategic and tactical plans for the asset(s) for the primary indication as well as new indications to expand into as part of the asset life cycle management. The Director should have a strong background and experience in the field of solid tumors, with proven ability to translate and align commercial and scientific goals and objectives into actions. Director will work as an integral part of the Medical Affairs Strategy Team in close alignment with Global Medical Affairs Strategy Lead and the cross-functional medical affairs cross functional partners, providing input and strategic direction for the program. Director will also support data generation and life cycle management initiatives as well as establish and maintain the relationships with the global thought leaders in support of the programs.

Requirements

Scientific or Medical Degree (Pharm D, PhD, MD) required
Expertise in clinical landscape of solid tumors required; Knowledge of gynecological cancers is preferred.
7+ years of medical affairs or clinical development background in oncology
Biotech / Pharmaceutical industry experience, with strong understanding of solid tumor drug development and medical affairs function
Ability to work successfully under pressure in a fast-paced environment and with tight timelines
Demonstrated ability to lead strategically, drive performance, build alignment, inform, negotiate, and collaborate across partnerships
Ability to lead collaboratively across various internal stakeholders and develop trusted partnerships
A strong ability to interpret and articulate clinical/HEOR data and the impact on development programs
In-depth understanding of compliance and regulatory requirements for pharmaceutical Medical Affairs, R&D and Commercial work
Knowledge of evidence-based medicine concepts, applied biostatistics and health economics are desirable
Demonstrated organizational skills to manage multiple projects simultaneously, prioritize projects effectively and communicate at all levels within the company
Strong written and verbal communication skills (including presentation skills)
Ability to travel locally and internationally to conferences and other meetings, which will include occasional weekend travel

Responsibilities

Lead annual medical planning for asset(s);
Work closely with extended medical affairs functions (global and regional markets) to inform and implement overall medical strategy for designated products and/or therapeutic areas
Lead and execute on engagement strategy with thought leaders, patient advocacy groups, professional societies and institutions
Lead the planning and execution of Early Access Program, and investigator initiated trials program, within appropriate standards for compliance, quality, timeliness, and budget - in alignment with MASL
Contribute and execute on the life cycle management of the asset (s)
Drive collaboration with cross-functional teams (e.g. commercial, field/regional, medical information/communication, HEOR) to provide support, medical review, and medical expertise advice as required
Collaborate with medical and clinical operations departments to coordinate the planning, execution, and management of clinical trial activities across medical affairs functions
Contribute to effective publication planning to ensure consistent and meaningful scientific communication
Contribute to the development of internal guidance and process/resource documents
Contribute to development and review of regulatory documents for regulatory submissions
Serve as medical reviewer and expert on promotional and medical review committees
Inform development of strategies to demonstrate the value of disease/products with focus on payer and clinical decision-maker outcomes
Lead the strategy team congress activity planning in collaboration with cross-functional stakeholders, and compiling of congress reports including key competitive intelligence
Lead and collaborate on cross-functional launch activities globally

Benefits

401(k) Plan: 100% match on the first 6% of contributions
Health Benefits: Two medical plan options (including HDHP with HSA), dental, and vision insurance
Voluntary Plans: Critical illness, accident, and hospital indemnity insurance
Time Off: Paid vacation, sick leave, holidays, and 12 weeks of discretionary paid parental leave
Support Resources: Access to child and adult backup care, family support programs, financial wellness tools, and emotional well-being support
Additional Perks: Commuter benefits, tuition reimbursement, and a Lifestyle Spending Account for wellness and personal expenses

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