Senior Director, Global Medical Affairs, Evidence Generation

This is a fully remote position, open to applicants in United States, +2 more countries.

📋 Description

• Oversee global MMN medical launch-readiness activities in collaboration with cross-functional and regional teams.

• Transform MMN evidence gaps into a comprehensive, data-driven global evidence strategy.

• Direct the medical strategy and provide scientific oversight for evidence-generation projects.

• Work alongside Clinical Development, RWE, HEOR, and regional MAEG teams.

• Convert global strategies into locally applicable plans and incorporate regional insights.

• Establish partnerships with experts, healthcare organizations, and patient advocacy groups.

• Identify and prioritize the educational and evidence needs throughout the patient journey.

• Assist in developing publication plans and medical education strategies in coordination with Scientific Communications.

• Maintain expertise in the relevant diseases and products from a scientific and medical perspective.

• Compile insights from scientific exchanges, regional teams, congresses, advisory boards, and patient communities into actionable recommendations.

• Provide medical and scientific insights into study concepts, protocols, feasibility assessments, investigator engagement, and recruitment challenges.

• Ensure compliance of medical affairs activities with pharmaceutical regulations and argenx policies.

• Participate in national and international meetings and congresses.

⛳️ Requirements

• An advanced degree is required: M.D., Ph.D., or PharmD.

• A minimum of 10 years of relevant experience is essential in Medical Affairs or a combination of Medical Affairs and closely related clinical development or evidence-generation roles, with significant leadership responsibilities in Medical Affairs.

• Experience in launching products in the neuromuscular/immunology field is mandatory.

• Proven experience in building empowered, high-performing teams and networks.

• Strong comprehension of drug development processes and the ability to critically assess clinical and scientific evidence.

• Demonstrated experience in creating and implementing integrated medical and evidence-generation strategies.

• Capability to translate evidence gaps into practical study concepts and critically analyze results.

• Experience collaborating with methodological experts and scientific communications teams on dissemination efforts.

• Ability to forge trusted scientific partnerships with medical professionals and other stakeholders.

• Exceptional verbal and written communication skills, including interpersonal communication and presentation abilities.

• Proficient in leading through influence, resolving cross-functional trade-offs, prioritizing resources, and achieving agreed outcomes within complex matrix teams.

• Willingness to travel approximately 30% internationally and domestically.

🏝️ Benefits

• Eligible for participation in short-term and long-term incentive programs, subject to plan terms and applicable policies.

• Comprehensive benefits package offered.

• Retirement savings plans available.

• Health benefits included.