
Senior Program Officer, Toxicology, Global Health
Bill & Melinda Gates Foundation
- Seattle, WA
- Permanent
- Full-time
Your RoleWe are currently seeking a Senior Program Officer (SPO), Toxicology, to join the Translation Sciences (TS) team within DTS. This role will contribute to a collaborative innovative culture and help accelerate the translation of research into practical health solutions, especially in resource-constrained environments. As we respond to a general need at the Foundation for acceleration across the entire discovery-development-regulatory-uptake space, it has become clear that we need to front-load toxicological evaluation in a concerted fashion early on in order to decrease the likelihood of later safety failures in human studies. The ideal candidate brings deep expertise in the current frontiers of toxicology and nonclinical safety assessment, paired with a passion for global health impact.This SPO will work cross-functionally with discovery scientists, pharmacologists, and product developers to apply modern translational toxicology thinking to global health R&D. They will support safe and efficient progression of candidate therapeutics, vaccines, and other biologics from preclinical models into human and patients' clinical studies, ensuring robust understanding of safety, tolerability, and pharmacologic liabilities.The successful candidate will also guide investment strategies, conduct technical due diligence, and cultivate partnerships with academic, not-for-profit, biotech, and pharmaceutical organizations.What You'll DoStrategy Development:Partner with the Deputy Director to shape strategies for nonclinical development of global health products.
Promote early integration of investigative toxicology into discovery programs and ensure alignment with clinical development plans.
Champion application of state-of-the-art safety and toxicology sciences approaches and regulatory strategy for innovative modalities.
Investment management:Manage a substantial portfolio of sophisticated investments (grants, contracts, equity investments) focused on toxicology, safety assessment, and preclinical development, requiring both relevant subject matter expertise and high-level leadership skills; including applying and evaluating milestone-based performance objectives and helping to make go/no-go decisions about specific projects and product candidates.
Identify and select partner institutions (e.g., academic, not-for-profit, biotech, pharma, PDP) as well as develop the scope and strategy for selected grants, investments, MoUs and contracts.
Serve as a thought partner and resource to grantees and partners to facilitate accomplishment of strategic objectives.
Contribute to review of proposals and write proposal summaries.
Keep Foundation colleagues advised of progress on individual grants and investments that may constitute solution sets for specific global health problems.
Source and evaluate potential new investments; lead due diligence and investment framing.
Provide Subject Matter Expertise:Provide toxicological expertise and guidance to internal teams and external partners.
Evaluate preclinical data packages and risk assessments across a range of modalities including small molecules, biologics, vaccines, and gene-based therapeutics.
Track innovations in predictive and mechanistic toxicology, in vitro and in silico modeling, and safety biomarker development.
Contribute to scientific learning and publications and represent the foundation in external forums.
Contribute to foundation knowledge capture, evaluation, learning, and dissemination; including developing reviews, summaries and informative reports that summarize key activities as well as supporting monitoring and evaluation activities.
Monitor and provide analysis on technology trends, innovations, and policy issues relevant to initiatives/portfolios.
Represent the Foundation externally and be recognized as thought leader through participation in public events and meetings related to area of expertise and position responsibilities, as well as through written work in relevant journals and publications.
Partnerships:Build and maintain strategic relationships with external partners including CROs, academic centers, biotech firms, and regulatory bodies.
Facilitate alignment of partner activities with foundation goals and ensure scientific and operational excellence.
Actively contribute to global scientific and regulatory discussions relevant to toxicology and safety science in global health.
Your ExperiencePhD, DVM, or equivalent in Toxicology, Pharmacology, or related discipline with 15+ years of experience in pharmaceutical or biotech sectors.
Extensive experience leading toxicology programs and contributing to the successful transition of therapeutics from preclinical to clinical development and to the market.
Proven expertise in GLP-compliant toxicology study design, interpretation, and regulatory documentation (e.g., IND/CTA/NDA/BLA preparation).
Familiarity with emerging safety science platforms (e.g., organ-on-chip, computational toxicology, high-content in vitro assays, AI).
Experience with small molecules, biologics, vaccines, and/or gene therapies preferred.
Strong leadership skills and demonstrated ability to influence and collaborate across scientific and organizational boundaries.
Global mindset and enthusiasm for applying scientific rigor to address health inequities in low-resource settings.
Exceptional written and verbal communication skills, scientific curiosity, and a commitment to team-based problem-solving.
Demonstrated excellence in scientific writing and data analysis, written and oral communication skills, and experience advocating and communicating with a broad and diverse audience.
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