Therapeutics Programmatic and Technical Advisor

Therapeutics Programmatic and Technical Advisor The Opportunity: To achieve an organization’s mission, leaders need strong team members who can develop innovative solutions, evaluate the latest technologies and strategic initiatives, and manage projects, programs, and portfolios. We are looking for a Therapeutics Programmatic and Technical Advisor to support multiple therapeutics innovation programs. The ideal candidate will have an advanced training in immunology or pharmacology, experience managing therapeutics development programs and thriving at the intersection of science, strategy, and program execution, and be motivated to accelerate the development of life-saving medical countermeasures (MCMs). As part of our team, you'll work with world-class scientists, technical experts, and public health professionals to support enabling technologies. Your attention to detail, flexibility, communication skills, understanding of the client's mission, and problem-solving will enable the mission's success. Our client supports the advanced research and development (R&D) of MCMs to protect Americans and respond to 21st-century national health security threats. They employ a comprehensive portfolio approach to address the public health consequences of CBRN events, pandemic influenza, and emerging infectious diseases. What You’ll Work On: Partner with a Project Officer to design, execute, and manage complex R&D programs. Help shape strategy, define technical direction, and operationalize programs from concept through execution. Provide feedback on drug development approaches, including R&D plans as well as regulatory and clinical strategies. Participate in market research efforts and conduct deep landscape analyses, including literature, market, and stakeholder engagement, to identify emerging technologies, gaps, opportunities, and potential players, and then translate insights into actionable program strategies and funding priorities. Contribute to the full lifecycle of program management, including acquisition package development, topic development, proposal evaluation, contract oversight, and performance monitoring, across a varied portfolio of performers. Provide scientific and technical insight across a portfolio of innovations focused on improving national health security. Perform additional duties related to programmatic support for MCM as assigned. Join us. The world can't wait. You Have: 8+ years of experience in biological or chemical sciences, life sciences, clinical studies, pharmaceutical industry regulatory affairs, quality assurance, quality control positions, clinical trials, or epidemiological research Experience using Microsoft 365 tools, including Teams and SharePoint Knowledge of therapeutic product development or early-stage biomedical product development Ability to support biological or biochemical research agendas Ability to obtain and maintain a Public Trust or Suitability/Fitness determination based on client requirements Doctorate degree in Biology, Chemistry, Biomedical Science, a Life Science field such as Immunology, Molecular Biology, Biochemistry, or Microbiology, or a Physical Science field such as Engineering, Physics, or CS Nice If You Have: 5+ years of experience in early-stage biomedical product development Experience with program or project management in a scientific, engineering, or biomedical field Knowledge of the health security and MCM innovation ecosystem Ability to synthesize complex information into clear, compelling narratives, including development of program materials, briefings, and stakeholder engagement Ability to manage multiple priorities, operate under tight timelines, and pivot quickly in a dynamic and collaborative environment Vetting: Applicants selected will be subject to a government investigation and may need to meet eligibility requirements of the U.S. government client.

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