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Prosidian Consulting

Management and operations consulting firm

Vaccine and Biologic Development SME - Healthcare and Life Sciences

Full-Time
No salary listed
Expert
PharmD, PhD, MD
Washington, DC, USA
In PersonWork is based in Washington, DC, with coverage across the Mid-Atlantic region.
Biology & BiotechRegulatory & Quality (Life Sciences)

About the job

Requirements
  • A doctoral degree in medicine or pharmacy, such as a PhD, MD, PharmD, or equivalent.
  • At least 10 years of experience in vaccine and biological drug development.
  • Subject matter expertise in vaccine and biological drug development, particularly regulatory studies and licensure programs.
  • Expertise in the advanced development and acquisition of vaccines and biological drugs within the Biomedical Advanced Research and Development Authority mission.
  • Experience applying regulatory frameworks to vaccine and biological drug development.
  • Knowledge of Food and Drug Administration approval processes, regulatory submissions, and licensure programs.
  • Expertise managing and overseeing vaccine and biological drug development from preclinical through clinical phases.
  • Understanding of biologic drug manufacturing, quality control, and testing procedures.
  • Expertise in data analysis and evaluation for regulatory submissions and clinical trials.
  • Ability to manage and guide regulatory studies, advanced development processes, and licensure programs.
  • Strong project management skills, including overseeing development phases, compliance, and adherence to timelines.
  • 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 the Biomedical Advanced Research and Development Authority mission.
  • Understanding and proficiency with business tools and technology, including Microsoft Office, Excel, Access, Outlook, PowerPoint, Word, Adobe Acrobat, data analytic tools, and Visio.
Responsibilities
  • Support Biomedical Advanced Research and Development Authority program offices as a subject matter expert in chemical, radiological/nuclear, burn and blast, biological, influenza, and emerging infectious disease threats, including the research, development, manufacture, and regulatory approval, licensure, or clearance of medical countermeasures.
  • Provide guidance and recommendations on key issues within the identified subject matter areas.
  • Serve as an advisor on Technical Evaluation Panels covering white papers, market research abstracts, technical proposals, and budget proposals.
  • Participate as a subject matter expert on Program Coordination Teams.
  • Provide expert assessments, recommendations, guidance, and educational material to Program Coordination Teams and the contracting officer's representative.
  • Provide subject matter expertise and advisory support to federal staff developing cost estimates for notional programs and proposed work.
  • Review and comment on study protocols, study reports, regulatory documents, presentations, proposals, solicitations, and post-award contract documents and deliverables.
  • Develop expert summary reports, expert opinion assessment reports, analysis reports, manuscript contributions, reviews, and technical assessments related to the Biomedical Advanced Research and Development Authority mission.
  • Advise federal staff on the appropriateness and probability of success of contractor-proposed statements of work and suggest improvements.
  • Distill complex information into concise summaries, including risk-benefit analyses and balanced recommendations.
  • Participate in strategic discussions with the United States Government to build new program areas aligned with the Biomedical Advanced Research and Development Authority mission.
  • Provide recommendations for project-development-level portfolio management and oversight.
  • Recommend, advise on, develop, implement, and improve Total Life Cycle Cost efforts.
  • Participate in market research efforts.
  • Provide guidance on regulatory strategies for vaccine and biologic drug development.
  • Work with Biomedical Advanced Research and Development Authority leadership on development strategies for current and future vaccine and biologic drug contracts.
  • Advise federal staff on cost estimates and resource requirements for proposed programs.
  • Advise on risk management, risk-benefit analysis, and strategic recommendations for vaccine and biologic drug development and acquisition.
  • Lead or participate in Technical Evaluation Panels, providing expert assessments on regulatory, clinical, and development aspects.
  • Ensure the successful completion of regulatory studies and licensure of vaccines and biological drugs.
Desired Qualifications
  • Experience in medicinal chemistry; preclinical development involving animal models, pharmacology, and toxicology; advanced clinical development involving medical officers, immunologists, and clinical operations; analytical product testing and test development; quality control; clinical or regulatory policy; manufacturing chemistry, manufacturing, and controls; process development, scale-up, and optimization; device development and manufacturing; reliability engineering; software; assay chemistry; microbiology; virology; immunology; plastic consumable design and manufacturing; manufacturing scalability and capacity expansion; sterile or aseptic technique; sterile manufacturing or filling; and sterile facilities and gowning.
  • Extensive experience in regulatory studies, licensure programs, and advanced vaccine and biological drug development.
  • Extensive experience working with vaccine and biologic drug manufacturers, the Food and Drug Administration, and other regulatory bodies.
  • Ability to manage large-scale, complex projects involving government, contractors, regulatory bodies, and other stakeholders.
  • Strong leadership and experience mentoring and advising federal teams, contractors, and stakeholders involved in vaccine and biologic drug development.

About the company

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

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Simplify Jobs

Simplify's Take

What believers are saying

  • ProSidian posted multiple NSF HR analytics roles in April 2026.
  • June 2026 contract data shows $4.0M obligated across repeat federal buyers.
  • GSA MAS validity through 2032 supports continued federal selling capacity.

What critics are saying

  • PrimeRFP shows 41% of obligations came from NSF in June 2026.
  • Eighty percent of obligations were not openly competed, risking renewal shocks.
  • Without new federal recompetes, the firm risks collapse from contract loss.

What makes Prosidian Consulting unique

  • ProSidian held a GSA MAS contract through May 17, 2032.
  • ProSidian sells federal consulting across NSF, DoD, DOE, and Treasury.
  • ProSidian positions itself in human capital, compliance, energy, and risk work.

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Benefits

  • Remote Work Options