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Senior Programmatic Technical Advisor_BARDA

Job in Vienna, Fairfax County, Virginia, 22184, USA
Listing for: Aveshka
Full Time position
Listed on 2025-12-27
Job specializations:
  • Research/Development
    Data Scientist, Research Scientist
Job Description & How to Apply Below

Senior Programmatic/Technical Advisor
Background: Softtek Government Solutions is looking for a Senior Program/Technical Advisor to support an HHS program — Critical Operations, Research & Expertise (CORE), Scientific and Programmatic Assistance Services — with ASPR/BARDA in Washington, DC.Personnel on the Critical Operations, Research & Expertise (CORE), Scientific and Programmatic Assistance Services contract will support BARDA in the various areas of interest within the Medical Countermeasures field of Research and Development (R&D)/Analytical Research and Development (AR&D) of biotechnology and biopharmaceuticals.

These services are critical in support of BARDA’s mission to conduct R&D and AR&D efforts to provide medical countermeasures that address the public health medical consequences of chemical, biological, radiological, and nuclear (CBRN) events, pandemic influenza, and emerging infectious diseases.
Duties/Responsibilities:

  • Provide expertise and advisory support related to medical countermeasures being utilized for federal public health emergency responses.
  • Provide advance services including but not limited to:
  • Data cleaning
  • Data transfers
  • Data quality control
  • Data integration and validation
  • Data analysis and report package preparation
  • Statistical simulation
  • Statistical toolbox for advanced data modelling, tabulation, and visualization. In addition, this position will provide ad hoc statistical support to BARDA projects under the guidance of BARDA statisticians.
  • Directs tasks and leads technical efforts and scientific projects. Acts as an SME on scientific subjects. Contributes subject matter expertise to programs with technical or program management expertise. Facilitates meetings as directed.
  • Provide advisory support to BARDA Program Division(s);
    Prepare draft work statements (SOW, SOO, PWS IGCE & Cost Estimates) for solicitations [Request for Information (RFIs), Request for Proposals (RFPs), Sources Sought Notices (SSN), et al].
  • Serve as advisor on Technical Evaluation Panels (TEPs) to include white papers/market research abstracts, technical proposals, and budget proposals.
  • Participate on Program Coordination Teams (PCTs)
  • Provide assessments, recommendations, and guidance as well as educational material to PCT and COR, as needed
  • Participate in strategic discussions, working with USG, in building new program areas in alignment with BARDA’s mission space.
  • Provide recommendations for project development level portfolio management and oversight as required.
  • Provide recommendations or advise on development, implement, and consciously improve Total Life Cycle Cost (TLCC) efforts;
    Participate in Market Research efforts.
  • Analyze protocols, study reports, regulatory documents, presentations, proposals, and related documents, as needed.
  • Additional duties related to programmatic support for MCM maybe assigned.

Required Qualifications and Experience

  • Understanding of medicinal chemistry; preclinical development (animal models, pharmacology, toxicology); advanced clinical development (medical officers, immunologists, clinical operations); analytical product testing and testing development; quality control; clinical and/or regulatory policy; and/or manufacturing (chemistry, manufacturing, and controls); process development, process scale-up and process optimization; device development and manufacturing, reliability engineering, Software, Assay chemistry, microbiology, virology, immunology.
  • Experience in manufacturing scalability and capacity expansion and sterile/aseptic technic, sterile manufacturing/filling and sterile facilities (sterile gowning). Plastic consumable design and manufacturing.
  • Provide guidance and recommendations on key issues related to the area(s) identified above.
  • Minimum of twelve (12) years of relevant industry experience with:
  • Doctoral degree in biological and/or chemical sciences with relevant postdoctoral experience OR
  • Clinical studies: application of doctoral degree(s) in medicine or pharmacy or with commensurate experience(s) advanced degree in computer science, Statistics, or related fields. Extensive knowledge and experience in clinical trials and epidemiological research including seven…
Position Requirements
10+ Years work experience
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