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Integrate, analyze, and interpret data from surveillance, clinical, and operational health systems to support public health decision-making, biosurveillance, and Air Force mission readiness. Apply epidemiology, biostatistics, and research methods to design studies, model outcomes, submit IRB protocols, and provide actionable intelligence to military leaders and public health professionals.

Design, develop, implement, and evaluate instructional programs, eLearning, multimedia, and training materials using ADDIE and instructional design best practices to support Air Force education and training missions.

Design and build dashboards and visualizations from integrated health, surveillance, and operational datasets to inform Air Force public health decision-makers. Perform data preparation, cleansing, modeling, analysis, and communicate insights to senior leaders while ensuring HIPAA-compliant handling of sensitive health information.

Ensure compliance with DAF/AFRL/DoD/NARA records and information governance policies, protect PII/CUI, support FOIA/Privacy Act processes, produce reports and briefings, deliver training, and drive process improvements to support leadership.

The FOIA Analyst manages FOIA and Privacy Act programs, processes requests, ensures compliance with laws, prepares reports, and handles administrative audits at the Department of the Air Force.

Provide financial, accounting, and administrative support for federal government operations, ensuring compliance with accounting practices and analyzing financial data.

Develop SAS programs for clinical data analysis, create CDISC-compliant datasets, validate programming outputs, and assist in regulatory submissions.

The Senior Technical Product Manager will oversee the lifecycle of FDA-regulated medical products, coordinating across teams to ensure compliance and successful commercialization.

The Protocol Specialist coordinates distinguished visitor engagements, events, and administrative tasks while ensuring adherence to military protocol standards.

As a Senior Regulatory Affairs Scientist, you will develop submission strategies, prepare regulatory documents, and liaise with regulatory agencies for medical products.