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Prosidian Consulting

Management and operations consulting firm

Vaccine and Biologic Development SME - Healthcare and Life Sciences

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeWashington, DC, USA

About the Job

Requirements

  • 10+ years of experience in vaccine and biological drug development SME work.
  • A doctoral degree in medicine or pharmacy (PhD, MD, PharmD, or equivalent).
  • Expertise in vaccine and biological drug development, particularly regulatory studies and licensure programs.
  • Expertise in advanced development and acquisition of vaccines and biological drugs within BARDA’s mission.
  • Experience applying regulatory frameworks to vaccine and biological drug development.
  • Knowledge of FDA 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 BARDA’s mission.
  • Extensive experience in regulatory studies, licensure programs, and advanced development in vaccines and biological drugs.
  • Strong leadership and experience mentoring and advising federal teams, contractors, and stakeholders involved in vaccine and biologic drug development.
  • Understanding and proficiency with business tools and technology, including Microsoft Office; advanced proficiency with Excel, Access, Outlook, PowerPoint, and Word; and proficiency with Adobe Acrobat, data analytic tools, and Visio, with the ability to quickly learn other tools as necessary.

Responsibilities

  • Support BARDA Program Offices as a subject-matter expert in chemical threats, radiological/nuclear threats, burn and blast injuries, biological threats (including viral and bacterial threats), influenza, and emerging infectious diseases, and in research, development, manufacture, and regulatory approval, licensure, or clearance of medical countermeasures, including diagnostics, medical devices and infrastructure, vaccines and other preventives, and therapeutics.
  • Provide guidance and recommendations on key issues in the identified expertise areas.
  • Serve as an advisor on Technical Evaluation Panels, including reviewing 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 as needed.
  • Provide subject-matter expertise and advisory support to federal staff developing cost estimates for notional programs or 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 or contributions, and reviews and technical assessments of documents related to BARDA’s mission, including solicitations, white papers, proposals, and post-award contract documents and deliverables, within the SME area and required expertise level.
  • Advise federal staff on the appropriateness and probability of success of contractor-proposed statements of work and suggest improvements.
  • Distill complex information into informative, concise summaries, including risk-benefit analyses and balanced recommendations.
  • Participate in strategic discussions with the U.S. Government to build new program areas aligned with BARDA’s mission.
  • Provide recommendations for project-development-level portfolio management and oversight as required.
  • Recommend or advise on developing, implementing, and improving Total Life Cycle Cost efforts, and participate in market research.
  • Provide guidance on regulatory strategies for vaccine and biologic drug development.
  • Contribute to or review regulatory submissions, study protocols, study reports, and proposals related to vaccine and biological drug development.
  • Work with BARDA leadership on development strategies for current and future contracts related to vaccines and biologic drugs.
  • 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.
  • Support successful completion of regulatory studies and licensure of vaccines and biologic drugs.
  • Review and comment on solicitations, proposals, and post-award contract documents.

Desired Qualifications

  • Experience in medicinal chemistry; preclinical development, including animal models, pharmacology, and toxicology; advanced clinical development, including medical officers, immunologists, and clinical operations; analytical product testing and testing development; quality control; clinical or regulatory policy; manufacturing, including 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 techniques; sterile manufacturing and filling; and sterile facilities and sterile gowning.
  • Deep understanding of regulatory pathways, clinical trials, and market approval for vaccines and biologic drugs.
  • Experience working with vaccine and biologic drug manufacturers, the FDA, and other regulatory bodies.
  • Ability to manage large-scale, complex projects involving government, contractors, and regulatory bodies.

About the Company

Prosidian Consulting

Management and operations consulting firm

ProSidian Consulting is a management and operations consulting firm that helps private companies, Fortune 1000 enterprises, and government agencies solve problems and improve operations through tailored, industry-aligned services. It offers six enterprise practice areas: Risk Management, Energy & Sustainability, Compliance, Business Process, IT Effectiveness, and Human Capital, delivered by multidisciplinary teams across CONUS/OCONUS. The firm follows a structured approach to strategic solutions focused on growth, margin, and efficiency, aligning assets, processes, policies, and people to deliver value. With former Big 4 leadership and a nationwide/overseas footprint, its goal is to translate strategy into execution that boosts clients' return on invested capital and value delivered to customers.

Company size
11-50
Company stage
Not listed
Total funding
Not listed
Headquarters
Charlotte, NC
Founded
2008

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