Full-Time

Senior Reg Ops Specialist 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
Operations & Logistics (1)
Required Skills
Word/Pages/Docs
Requirements
  • Bachelor’s degree or equivalent qualification in a relevant field
  • At least 15 years of progressive experience in regulatory operational activities supporting FDA-regulated product development
  • Deep expertise in FDA submission types, eCTD specifications, and advanced regulatory operations
  • Strong leadership in submission management
  • Superior competency in MS Word, Adobe Acrobat, and PDF toolsets (e.g., ™)
  • Experience with electronic publishing software (e.g., Lorenz or similar tools) and XML document creation
  • Advanced knowledge of FDA and ICH submission requirements
  • Ability to self-train in specialized areas (e.g., CSR publishing, PEUA, EUA)
  • Strong project management skills for submission coordination and timeline management
  • Ability to design, review, and archive eCTD submissions, including original filings and amendments
  • Knowledge of FDA regulatory frameworks, guidelines, and operational requirements
  • Exceptional attention to detail in formatting, publishing, and dossier preparation
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 technic, 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(s) on Technical Evaluation Panels (TEPs) to include 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 but not limited to expert summary reports, expert opinion assessment reports, analysis reports, manuscript writing/contribution, and review and technical assessments on a wide variety of documents related to BARDA’s mission, including solicitations, white papers, proposals, and post-award contract documents and deliverables), as requested in their SME area and at their required level of expertise.
  • Advise federal staff on the appropriateness and the probability of success of Contractor proposed statements of work Make suggestions on ways to improve those statements of work.
  • Experience distilling complex information into informative and concise summaries, including providing risk/benefit analyses and balanced recommendations.
  • Participate and aid 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.
  • Follow FDA submission requirements in consideration of BARDA Program Divisions and the regulatory operational requirements of BARDA core services including clinical, nonclinical, and manufacturing network services.
  • Provide subject matter expertise for the management, design, publishing, review, submission, and archive of eCTD submissions, including amendments and original filing.
  • Coordinate publishing and submitting of all electronic dossiers and documents to regulatory authorities and/or clients.
  • Liaise with Regulatory Affairs Project Managers, and CROs directly, as necessary, to coordinate submission timelines and technical specifications and for client eCTD reviews.
Desired Qualifications
  • Bachelor’s degree or equivalent qualification.
  • At least 15 years of progressive experience in regulatory operational activities supporting FDA-regulated product development.
  • Deep expertise in FDA submission types, eCTD specifications, and advanced regulatory operations.
  • Strong leadership in submission management
  • Additional certifications or training in regulatory operations and publishing software preferred
  • Experience with electronic publishing software (e.g., Lorenz or similar tools) and XML document creation
  • Advanced knowledge of FDA and ICH submission requirements
  • Ability to self-train in specialized areas (e.g., CSR publishing, PEUA, EUA)
  • Strong project management skills for submission coordination and timeline management
  • Ability to design, review, and archive eCTD submissions, including original filings and amendments
  • Knowledge of FDA regulatory frameworks, guidelines, and operational requirements
  • Exceptional attention to detail in formatting, publishing, and dossier preparation

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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