Full-Time

Senior Vaccine and Biologic Development SME

Healthcare and Life Sciences

Prosidian Consulting

Prosidian Consulting

11-50 employees

Management and operations consulting firm

No salary listed

Washington, DC, USA

In Person

Category
Consulting (2)
,
Required Skills
Medicinal Chemistry
Microbiology
Pharmacology
Requirements
  • Doctoral degree(s) in medicine or pharmacy (PhD, MD, PharmD, or equivalent)
  • Extensive experience in regulatory studies, licensure programs, and advanced development in vaccines and biological drugs
  • Experience in the application of regulatory frameworks for vaccine and biological drug development
  • Knowledge of the FDA approval processes, regulatory submissions, and licensure programs
  • Expertise in data analysis and evaluation for regulatory submissions and clinical trials
  • Strong project management skills, including overseeing development phases, compliance, and adherence to timelines
  • Experience distilling complex information into informative and concise summaries, including risk/benefit analyses and balanced recommendations
  • Deep understanding of regulatory pathways, clinical trials, and market approval for vaccines and biologic drugs
  • Experience working with vaccine and biologic drug manufacturers, FDA, and other regulatory bodies
  • Ability to manage large-scale, complex projects that involve multiple stakeholders (e.g., government, contractors, regulatory bodies)
  • Ability to manage regulatory studies, advanced development processes, and licensure programs
  • Ability to guide federal teams in aligning new program areas with BARDA’s mission
Responsibilities
  • Support BARDA Program Office(s) as a subject matter expert in the fields of Chemical Threats, Radiological/Nuclear Threats, Burn and Blast Injuries, or Biological Threats (including viral and bacterial threats), Influenza and Emerging Infectious Diseases Division (IEIDD) as well as the research, development, manufacture, and regulatory approval/ licensure/ clearance of medical countermeasures against these threats including but not limited to diagnostics and other medical devices/infrastructure vaccines and other preventives, and therapeutics.
  • Candidates with experience in 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. Plastic consumable design and manufacturing. Experience in manufacturing scalability and capacity expansion and sterile/aseptic technique, sterile manufacturing/filling and sterile facilities (sterile gowning). Provide guidance and recommendations on key issues related to the area(s) identified above.
  • Serve as advisor on Technical Evaluation Panels (TEPs) including white papers/market research abstracts, technical proposals, and budget proposals.
  • Participate as subject matter experts on Program Coordination Teams (PCTs)
  • Provide expert assessments, recommendations, and guidance as well as educational material to PCT and COR as needed
  • Provide subject matter expertise and advisory support to federal staff for development of cost estimates for notional programs/proposed work
  • Review and comment on study protocols, study reports, regulatory documents, presentations, proposals, and related documents.
  • Develop work products including expert summary reports, expert opinion assessment reports, analysis reports, manuscript writing/contribution, and review and technical assessments on BARDA documents and deliverables
  • Advise federal staff on the appropriateness and probability of success of Contractor proposed statements of work; make suggestions to improve statements of work.
  • Experience distilling complex information into summaries including risk/benefit analyses and balanced recommendations.
  • Participate in strategic discussions with US Government in building new program areas aligned with BARDA mission.
  • Provide recommendations for project development level portfolio management and oversight as required.
  • Provide recommendations or advice on development, implement, and enhance Total Life Cycle Cost efforts; participate in Market Research efforts.
Desired Qualifications
  • 15+ years for Senior Vaccine and Biological Drug Development SME
  • Subject Matter Expert (SME) in vaccine and biological drug development, particularly in regulatory studies and licensure programs
  • Doctoral degree(s) in medicine or pharmacy (PhD, MD, PharmD, or equivalent)
  • Extensive experience in regulatory studies, licensure programs, and advanced development in vaccines and biological drug
  • Experience in the application of regulatory frameworks for vaccine and biological drug development
  • Knowledge of the FDA approval processes, regulatory submissions, and licensure programs
  • Expertise in data analysis and evaluation for regulatory submissions and clinical trials
  • Deep understanding of regulatory pathways, clinical trials, and market approval for vaccines and biologic drugs
  • Experience working with vaccine and biologic drug manufacturers, FDA, and other regulatory bodies
  • Ability to manage large-scale, complex projects that involve multiple stakeholders (e.g., government, contractors, regulatory bodies)
  • Strong project management skills, including overseeing development phases, compliance, and adherence to timelines
  • Excellent communication and reporting skills for technical documents, proposals, and presentations
  • Ability to provide expert assessments and strategic advice on vaccine and biologic drug development projects
  • Ability to guide federal teams in aligning new program areas with BARDA’s mission

ProSidian Consulting provides management and operations consulting to private companies, Fortune 1000 enterprises, and government agencies. It uses industry-aligned services across six practice areas: Risk Management, Energy & Sustainability, Compliance, Business Process, IT Effectiveness, and Human Capital, delivered by multidisciplinary teams. The firm connects strategy to execution with On-Demand Resources and targets drivers of economic profit—growth, margin, and efficiency—across assets, processes, policies, and people. Its goal is to help leaders design and execute operations that increase value for customers and improve return on invested capital.

Company Size

11-50

Company Stage

N/A

Total Funding

N/A

Headquarters

Charlotte, North Carolina

Founded

2008

Simplify Jobs

Simplify's Take

What believers are saying

  • Remote-first model attracts talent nationwide, cuts office overhead costs.
  • Energy & Sustainability practice meets tightening ESG mandates for Fortune 1000.
  • Human Capital solutions address 2025-2026 retention, skills gaps challenges.

What critics are saying

  • Deloitte poaches Big 4 alumni, erodes 190-professional talent pool in 6-12 months.
  • Stagnant website since 2020 loses clients to Booz Allen in 3-6 months.
  • No alliances post-2013 isolates energy bids against EY networks in 6-12 months.

What makes Prosidian Consulting unique

  • On-demand model deploys experienced-only Big 4 alumni for rapid execution.
  • Multidisciplinary teams span Risk Management, Energy & Sustainability, Compliance.
  • Structured approach links strategy to execution across assets, processes, people.

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