Director Transgenic Mouse Jobs (NOW HIRING)

Portfolio & Program Management

• Lead and coordinate a portfolio of concurrent research programs spanning multiple principal investigators, timelines, and funding mechanisms.

• Develop, implement, andmaintainprogram management tools including project plans, milestone trackers, risk registers, and dashboards.

• Facilitate cross-functional team meetings, track action items, and ensure accountability across scientific and administrative stakeholders.

• Identifyand resolve operational bottlenecks and interdependencies that may affect program timelines or scientific deliverables.

• Support strategic planning efforts, including program prioritization, resource allocation, and go/no-go decision frameworks.

NIH Grant Administration & Reporting

• Serve as the program-level point of contact for large NIH grants (e.g., R01, P01, U01, U54, RM1), coordinating all administrative and scientific reporting requirements.

• Prepare, compile, andsubmitannual Progress Reports (RPPRs), non-competing renewals, supplements, and other required NIH correspondence.

• Monitor grant budgets, expenditure timelines, and ensure compliance with NIH terms and conditions in coordination with sponsored research offices.

• Track deliverables, milestones, and publication requirements across multi-project and multi-site awards.

• Coordinate with NIH Program Officers and other agency contacts as needed to address administrative or scientific programmatic matters.

Grant Writing & Scientific Communication

• Write, edit, and contribute to all sections of grant applications including Specific Aims, Research Strategy, human subjects/vertebrate animal sections,biosketches, and resource/environment pages.

• Prepare white papers, concept papers, letters of intent, and responses to RFAs/PAs across NIH and other federal or private funding agencies.

• Draft scientific summaries, program highlights, and lay-language communications for institutional and external audiences.

• Support manuscript preparation, including literature reviews,methodssections, and figure/table organization for peer-reviewed publications.

Scientific Contribution - Mouse Genetics & Therapeutic Development

• Provide scientific input and oversight on programs involving mouse genetics, including transgenic, knock-in, knock-out, and conditional models.

• Contributeexpertisein preclinical therapeutic development pipelines, including target identification, in vivo efficacy studies, and translational modeling.

• Critically evaluate experimental designs, interpret results, and ensure scientific rigor across program deliverables.

• Engage with scientific collaborators and external partners (academic, industry, and government) to advance program goals.

• Stay current with literature and emerging methodologies relevant to mouse genetics, neuroscience, rare disease, or other applicable therapeutic areas.

Compliance, Regulatory & Operational Oversight

• Ensure all animal research activities are conducted in compliance with IACUC protocols, institutional policies, and NIH guidelines.

• Support IRB submissions and renewals where applicable.

• Coordinate vendor management, subcontract oversight, and data sharing agreements associated with funded programs.

• Train and mentor junior program staff and research coordinators on project management best practices and grant administration procedures.

Required Qualifications

• Master's Degreerequired, but strong preference for aPh.D. in Genetics, Molecular Biology, Neuroscience, Pharmacology, or a closely related biomedical science field.

• Minimum of 5 years of experience in a research environment, with at least 2 years in a program management or research administration capacity.

• Demonstratedexpertisein mouse genetics, including design and interpretation of genetic mouse models (transgenic, CRISPR-based, conditional knockouts, etc.).

• Direct experience with NIH grant mechanisms and administration, including preparation of RPPRs, competitive renewals, and budget management.

• Proventrack recordas a scientific writer with experience authoring or co-authoring NIH grant applications and/or peer-reviewed publications.

• Strong organizational skills with the ability to manage multiple programs simultaneously under competing deadlines.

• Excellent interpersonal and communication skills; ability to work effectively with diverse teams of scientists, clinicians, and administrators.

Preferred Qualifications

• Experience in therapeutic development, drug discovery, or translational research programs,particularly inneuroscience or rare/genetic diseases.

• Familiarity with NIHeRACommons, Grants.gov, and related submission platforms.

• Prior experience managing multi-site or consortium grants (e.g., P01, U54, U19).

• Knowledge of GLP/GCP principles and preclinical regulatory frameworks.

• Postdoctoral research experience with independent publicationrecord.

• Experience with project management software (e.g., Smartsheet, Asana, MS Project) and data visualization tools.

• Established network of collaborators in academic or industry research settings.

Core Competencies