Science & Business Development Lead
Job Summary
Battelle is seeking a nationally recognized scientific leader in New Approach Methodologies (NAMs) to accelerate the adoption of human-relevant, non-animal testing platforms across research, safety assessment, and regulatory science.
Responsibilities
Develop and lead Battelle’s scientific strategy for integrating NAMs, MPS, organ-on-chip platforms, and human-relevant in vitro models into client programs.
Serve as a thought leader on emerging scientific and regulatory expectations across FDA, EPA, NIH/NICEATM, and industry sectors.
Translate technological advances into actionable programmatic growth opportunities.
Lead multidisciplinary scientific teams in the design, validation, and application of MPS technologies, including multi-organ and tissue-specific systems.
Establish integrated MPS workflows that incorporate transcriptomics, proteomics, metabolomics, and other omics-based platforms.
Develop approaches for MPS-to-in vivo extrapolation and computational toxicology integration (QSAR, machine learning, predictive modeling).
Provide scientific oversight, technical review, and quality assurance for complex R&D programs.
Collaborate with regulatory leaders to support scientific acceptance, qualification, and guidance development for MPS-based methodologies.
Represent Battelle in national working groups, interagency collaborations, scientific advisory committees, and industry consortia.
Build strategic partnerships with academic institutions, federal agencies, and industry leaders to expand MPS and NAM capabilities.
Contribute to proposal development, client engagement, and technical marketing to grow Battelle’s NAM/MPS portfolio.
Publish high-impact scientific manuscripts and present research findings at national and international conferences.
Key Qualifications
PhD (or equivalent) in toxicology, biomedical engineering, physiology, pharmacology, microbiology, virology, or related field.
Recognized subject-matter expertise in NAMs, MPS, organ-on-chip technologies, or advanced in vitro models.
Demonstrated leadership of interdisciplinary scientific teams.
Evidence of scientific impact through publications, regulatory engagements, working group participation, or technology development.
Experience applying human-relevant test systems to safety assessment, mechanistic investigation, or translational science.
Preferred Qualifications
Experience developing or validating MPS systems for regulatory applications (FDA, EPA, industry).
Participation in national NAM/MPS initiatives, interagency workgroups, or scientific standards development.
Familiarity with computational toxicology, QSAR modeling, and machine-learning approaches.
Proven ability to build collaborative partnerships and secure external funding.