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Moderna

Develops mRNA-based medicines for health

Head of Translational Medicine

Translational Research & Bench Biology +1Confirmed live in the last 24 hours
Full-timeCambridge, MA, USA

About the Job

Requirements

  • An advanced degree (PhD, MD, PharmD, or equivalent) in a relevant scientific discipline.
  • At least 15 years of experience across translational science, clinical pharmacology, and/or drug development, including at least 10 years in a leadership role.
  • Deep expertise spanning translational medicine, biomarker strategy, experimental medicine, and quantitative pharmacology.
  • Ability to develop scientific hypotheses on human disease and translate them between the clinic and the laboratory.
  • Demonstrated success influencing development strategy, including dose selection, study design, and regulatory interactions.
  • Strong understanding of the end-to-end drug development process, from discovery through commercialization.
  • Strong publication record and ability to represent the company externally to the scientific community.
  • Proven ability to lead large multidisciplinary teams and operate effectively in a complex matrix environment.
  • Experience mentoring, hiring, and growing talented scientists.
  • Track record of driving innovation and delivering measurable impact across a portfolio.
  • Ability to translate complex science into strategic decisions.
  • Employment is contingent on the ability to access export-controlled information in accordance with U.S. law; candidates who are not U.S. citizens, lawful permanent residents, asylees, or refugees may be considered contingent on obtaining a required export-control license.

Responsibilities

  • Define and lead an integrated, end-to-end translational strategy across Translational Medicine, Translational Research, and Clinical Pharmacology/Pharmacometrics, spanning discovery through lifecycle management.
  • Establish a unified framework connecting biological insights, biomarkers, and quantitative pharmacology to enable rapid, data-driven decision-making.
  • Align translational strategies with program and portfolio objectives, including development pathways, target product profiles, and regulatory strategies.
  • Lead translational input into governance and ensure rigorous, data-driven go/no-go decisions across the pipeline.
  • Lead and unify a high-performing, multidisciplinary translational organization, connecting scientific, clinical, and quantitative capabilities into a cohesive, integrated model.
  • Serve as a senior leader and thought partner across Research and Development, influencing strategy, prioritization, and execution.
  • Represent the company's translational strategy externally, engaging regulators, scientific leaders, and partners to shape scientific direction and advance approaches across the portfolio.
  • Lead execution of early clinical translational plans, including biomarker implementation, endpoint operationalization, and data interpretation to enable proof-of-concept decisions.
  • Partner with clinical development to translate scientific hypotheses into actionable clinical strategies and high-quality study execution.
  • Define and validate novel endpoints and patient stratification approaches to enable early decision-making and differentiation.
  • Serve as a senior clinical leader in internal and external settings, including study teams, governance, and interactions with investigators and key opinion leaders.
  • Build and advance translational capabilities, including molecular assays, sequencing, immune monitoring, and companion diagnostics, to enable patient selection and mechanistic insight.
  • Oversee generation and delivery of stage-appropriate translational data packages to support IND readiness and early clinical development.
  • Drive forward and reverse translation so clinical insights inform discovery, platform innovation, and next-generation therapeutics.
  • Lead development of patient identification, pharmacodynamic, and disease monitoring strategies to support clinical entry and advancement.
  • Drive quantitative integration of PK/PD, exposure-response, and modeling and simulation into program-level decision-making and trial design.
  • Lead pharmacology contributions to regulatory strategy, including authorship and defense of clinical pharmacology components in health authority interactions.
  • Ensure innovative application of pharmacometrics to dose prediction, first-in-human studies, and lifecycle optimization across the pipeline.
  • Represent clinical pharmacology in governance and partner cross-functionally to inform critical dose and development decisions across programs.

Desired Qualifications

  • Experience with companion diagnostics.
  • Leadership roles contributing to BLAs for oncology or immunology programs.
  • Deep expertise in immunology, oncology, and autoimmune disease.
  • A network of external academic experts.

About the Company

Moderna

Develops mRNA-based medicines for health

Moderna develops medicines built on messenger RNA (mRNA). Its products use mRNA delivered into cells to instruct them to produce specific proteins that can prevent or treat disease, with vaccines being a primary example. In practice, a dose delivers engineered mRNA into the body, cells translate it into a target protein, and the immune system responds or the protein modulates biology to combat disease. Moderna differentiates itself through its focus on building a whole mRNA medicines platform and in-house capabilities for designing, manufacturing, and scaling mRNA therapies, including rapid development and large-scale production. Its goal is to create a new category of medicines based on mRNA that can improve how diseases are discovered, developed, and treated, ultimately improving patient outcomes.

Company size
5,001-10,000
Company stage
IPO
Headquarters
Cambridge, MA
Founded
2010

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