jobs.pl/Пропозиції роботи/Дослідження та розробки/Senior Director, Global Regulatory Strategy, Oncology
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Senior Director, Global Regulatory Strategy, Oncology

Повна зайнятість Гібридна робота

Дата публікації: 01.09.2026

Moderna is seeking an individual to lead development and execution of global regulatory strategy for programs in its oncology portfolio. This leader will shape regulatory pathways for novel, first-in-class therapeutics and drive successful global development and registration strategies.

Responsibilities

Lead global regulatory strategies from early development through commercialization; Drive regulatory submissions (INDs, CTAs, BLAs/MAAs) with excellence and urgency; Lead health authority interactions (FDA, EMA, PMDA), including high-stakes negotiations; Shape strategies for novel and first-in-class therapies; Partner cross-functionally and across alliances to align on strategy; Anticipate regulatory risks and proactively mitigate them; Build and develop high-performing regulatory teams

Requirements

BA/BS degree in a scientific/engineering discipline; 12+ years of experience in the Pharmaceutical industry; 8+ years of experience in Regulatory strategy, including oncology; Strong knowledge of current US and EU regulations, including specifically: e.g. novel regulatory pathways.; Strong experience with CTD format and content regulatory filing; Exceptional written and oral communication; Experience with developing and implementing competitive regulatory strategies; Demonstrated track record in securing product approvals and maintaining a complex portfolio; Experience dealing with broad range of stakeholders at all levels internal and external to the company; Demonstrated competence in employee management and development; Knowledge of and broad experience with regulatory procedures and legislation for drug development, product registration, line extension and license maintenance – preferably from at least both US and EU; Direct experience of leading regulatory authority meetings in different phases of drug development

Nice to have

Graduate degree in a scientific discipline or other relevant graduate discipline or professional certification; Delivery of at least one major application (NDA/BLA/MAA/JNDA etc.); Acts with urgency and delivers results with excellence; Thinks and operates as an enterprise leader; Challenges convention and drives innovation; Makes high-quality decisions under ambiguity and pressure; Builds and develops high-performing, accountable teams; Influences effectively across internal and external stakeholders

Benefits

Competitive healthcare, plus voluntary benefit programs; A holistic approach to well-being, with access to fitness, mindfulness, and mental health support; Family planning benefits, including fertility, adoption, and surrogacy support; Generous paid time off, including vacation, volunteer days, sabbatical, global recharge days, and a discretionary year-end shutdown; Savings and investments to help you plan for the future; Location-specific perks and extras; The successful candidate may be eligible for an annual discretionary bonus, other incentive compensation, or equity award
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