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Prosidian Consulting

Management and operations consulting firm

Clinical Operations SME - Healthcare and Life Sciences

Full-Time
No salary listed
Senior
Bachelor's
Washington, DC, USA
In PersonWork is located in Washington, DC and across the Mid-Atlantic region.
Biology & BiotechClinical Research Operations

About the job

Requirements
  • At least 5 years of clinical trial operations experience beyond an advanced degree.
  • Experience in observational and Phase I-IV clinical trials.
  • Experience in a clinical research organization, pharmaceutical company, academia, private research organization, or government.
  • An advanced degree in medicine, nursing, pharmacy, biotechnology, or a related field.
  • Expertise in clinical trial operations, including observational and Phase I-IV trials.
  • Expertise in registrational Phase II/III trials for Senior SME candidates.
  • Ability to manage timelines, budgets, and deliverables with minimal oversight.
  • Experience developing, authoring, and reviewing Requests for Task Orders and evaluating Clinical Research Organization proposals.
  • Familiarity with Food and Drug Administration regulatory submission processes, guidelines, and document reviews.
  • Strong project management and clinical team leadership skills.
  • Proficiency in risk assessment and mitigation strategies for Senior SME candidates.
  • Strong analytical skills to monitor, assess, and course-correct contractors and vendors.
  • Ability to manage project timelines and budgets to ensure regulatory compliance and high-quality output.
  • Significant clinical operations leadership experience, including executive-responsibility roles, for Senior SME candidates.
Responsibilities
  • Support BARDA program offices as a subject-matter expert in chemical, radiological/nuclear, burn and blast, biological, influenza, and emerging infectious disease threats, as well as 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 materials 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, and related documents.
  • Develop expert summary reports, expert opinion assessment reports, analysis reports, manuscript contributions, and technical assessments of 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 United States Government to build new program areas aligned with BARDA's 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 clinical development subject-matter expertise to BARDA medical countermeasure programs.
  • Oversee and review clinical studies, regulatory submissions, and study-specific documents such as invoices.
  • Develop independent cost, resource, and timeline estimates when required for Senior SME work.
  • Prepare and manage project timelines and budgets to ensure regulatory compliance and high-quality output.
Desired Qualifications
  • Experience in medicinal chemistry.
  • Experience in preclinical development, including animal models, pharmacology, and toxicology.
  • Experience in advanced clinical development, including medical officers, immunologists, and clinical operations.
  • Experience in analytical product testing and test development.
  • Experience in quality control.
  • Experience in clinical or regulatory policy.
  • Experience in manufacturing chemistry, manufacturing, and controls.
  • Experience in process development, process scale-up, and process optimization.
  • Experience in device development and manufacturing.
  • Experience in reliability engineering.
  • Experience in software, assay chemistry, microbiology, and virology.
  • Experience in immunology.
  • Experience in plastic consumable design and manufacturing.
  • Experience in manufacturing scalability and capacity expansion.
  • Experience in sterile or aseptic technique, sterile manufacturing and filling, sterile facilities, and sterile gowning.
  • Familiarity with BARDA products and advanced development contracts involving vaccines, therapeutics, diagnostics, and devices.

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'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