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Prosidian Consulting

Management and operations consulting firm

Senior Vaccine and Biologic Development SME

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

About the Job

Requirements

  • At least 15 years of experience for the Senior Vaccine and Biological Drug Development SME role.
  • Subject matter 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.
  • A doctoral degree in medicine or pharmacy (PhD, MD, PharmD, or equivalent).
  • Extensive experience in regulatory studies, licensure programs, and advanced vaccine and biological drug development.
  • 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.
  • 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.
  • Experience working with vaccine and biologic drug manufacturers, the FDA, and other regulatory bodies.
  • Ability to manage large-scale, complex projects involving multiple stakeholders, including government, contractors, and regulatory bodies.
  • Microsoft Office proficiency, including advanced Excel, Access, Outlook, PowerPoint, and Word; proficiency with Adobe Acrobat, data analytics tools, and Visio; and ability to learn other tools as needed.

Responsibilities

  • Support BARDA program offices as a subject matter expert in chemical threats, radiological and nuclear threats, burn and blast injuries, biological threats including viral and bacterial threats, influenza, emerging infectious diseases, and the research, development, manufacture, and regulatory approval, licensure, or clearance of medical countermeasures, including diagnostics, medical devices and infrastructure, vaccines, other preventives, and therapeutics.
  • Provide guidance and recommendations on key issues in relevant subject-matter areas, including medicinal chemistry; preclinical development such as animal models, pharmacology, and toxicology; advanced clinical development; analytical product testing and testing development; quality control; clinical and 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; and sterile/aseptic techniques, sterile manufacturing and filling, sterile facilities, and sterile gowning.
  • Serve as an advisor on Technical Evaluation Panels, 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 Contracting Officer Representatives as needed.
  • Provide federal staff with subject matter expertise and advisory support in developing cost estimates for notional programs and proposed work.
  • Review and comment on study protocols, study reports, regulatory documents, presentations, proposals, and related documents.
  • Develop requested work products in the SME’s area and at the required expertise level, including expert summary reports, expert opinion assessment reports, analysis reports, manuscript contributions, and reviews and technical assessments of BARDA-related solicitations, white papers, proposals, and post-award contract documents and deliverables.
  • 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 U.S. Government to build 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 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 of 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; analytical product testing and testing development; quality control; clinical and/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/aseptic technique, sterile manufacturing and filling, sterile facilities, and sterile gowning.
  • Strong communication and reporting skills for technical documents, proposals, and presentations.
  • Strong leadership and experience mentoring and advising federal teams, contractors, and stakeholders involved in vaccine and biologic drug development.

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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