Field Medical Advisor, Oncology

The Field Medical Advisor role is pivotal in establishing and nurturing relationships within the oncology medical community, including healthcare practitioners (e.g. oncologists, surgical oncologists), policy makers, payers, patient groups, and healthcare administrators to advance understanding of our science and gather insights from across the healthcare ecosystem. This role enhances patient outcomes through the peer-to-peer scientific exchange of Moderna’s mRNA platform science, fostering trust through personalized and digital engagement. The Field Medical Advisor plays a key role in strengthening Moderna's scientific presence and translating these insights into actions that benefit HCPs and their patients. In this role, you will be at the forefront of Moderna’s mission to deliver new mRNA-based therapies across oncology indications, requiring a blend of scientific expertise, strategic thinking, strong internal collaboration, and a commitment to ethical engagement. We value curiosity, resilience, and the ability to adapt and innovate in a dynamic environment.

Responsibilities

Develop and execute territory engagement plans aligned to medical priorities; Utilize excellent verbal and written communication skills to simplify complex scientific topics and engage stakeholders; Gather and report meaningful customer insights to inform medical strategy; Engage with key stakeholders across the healthcare ecosystem; Engage in rich scientific dialogue about Moderna’s mRNA platform and oncology programs; Collaborate with clinical development and research teams to support clinical trials and research collaborations; Collaborate across Moderna and the healthcare ecosystem to enhance patient care and outcomes; Execute medical engagement activities including advisory boards, partnerships, round tables, and conferences; Adhere to ethical standards and protocols, document work in CRM, report adverse events and product quality complaints.

Requirements

Terminal degree in a Scientific Discipline (MD, PhD, PharmD) or equivalent is required; Minimum of 3 years of relevant clinical, research, therapeutic area, or disease-area experience beyond the terminal degree; Ability to conduct peer to peer level scientific discussion with key external stakeholders; Demonstrated scientific excellence and strong focus on scientific education and dialogue; Excellent stakeholder management, communication, networking and presentation skills; Ability to work independently, organize priorities, and operate effectively in a changing field environment; Understanding of pharmaceutical industry compliance expectations, including laws, regulations, ethical guidelines, and company policies; Fluency in English (both written and spoken); Familiarity with local regulatory environment and a basic understanding across other key regions (e.g. FDA, EMA, and other regional health authorities); Proficiency in digital technology (Microsoft Office Suite) and agility with virtual presentation platforms (e.g. MS Teams, Zoom, Webex); Understanding of the process and need for thorough and timely documentation in a CRM system; Ability to travel up to 75% as required.

Nice to have

Prior experience in melanoma (research, clinical, or medical affairs); Prior experience in immuno-oncology; Prior experience working with partnered and/or co-developed programs; Scientific and/or medical publication record preferred; Field-based medical or Medical Science Liaison (MSL) experience preferred; Proven ability to develop and manage KOL relationships and execute strategic territory engagement plans; Advanced proficiency in scientific dialogue, empathetic listening, and gathering actionable medical insights; Established relationships within the oncology medical community and a strong understanding of the healthcare ecosystem, including policy and regulatory agencies that influence patient care; Demonstrated ability to navigate compliance requirements while building trusted stakeholder relationships; Knowledge of health economics and real-world data/evidence (RWD/RWE), with the ability to engage in scientific discussions on these topics; Experience using digital-first approaches for stakeholder engagement, including AI-enabled tools and innovative platforms.

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; Annual discretionary bonus, other incentive compensation, or equity award (subject to company plan eligibility criteria and individual performance).