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Prosidian Consulting

Management and operations consulting firm

Clinical Operations SME - Healthcare and Life Sciences

Clinical Research OperationsConfirmed live in the last 24 hours
Full-timeWashington, DC, USA

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, pharma, academia, private research organizations, 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.
  • Ability to manage timelines, budgets, and deliverables with minimal oversight.
  • Experience developing, authoring, and reviewing Request for Task Orders (RTORs) and evaluating Clinical Research Organization (CRO) proposals.
  • Familiarity with FDA regulatory submission processes, guidelines, and document reviews.
  • Proficient risk assessment and mitigation strategies for Senior SME candidates.
  • Strong analytical skills to monitor, assess, and course-correct contractors and vendors.
  • Familiarity with BARDA products and advanced development contracts in vaccines, therapeutics, diagnostics, and devices is a plus.
  • Proficiency with Microsoft Office, including Excel, Access, Outlook, PowerPoint, and Word; Adobe Acrobat, data analytics tools, and Visio are also identified, with ability to quickly learn other tools.

Responsibilities

  • Support BARDA Program Offices as a subject matter expert in chemical, radiological/nuclear, burn and blast, biological, influenza, and emerging infectious disease threats, and in research, development, manufacture, and regulatory approval, licensure, or clearance of medical countermeasures including diagnostics, medical devices, vaccines, preventives, and therapeutics.
  • Provide guidance and recommendations on issues in relevant subject-matter areas.
  • Serve as an advisor on Technical Evaluation Panels, including review of 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 requested work products, including expert summary reports, expert opinion assessment reports, analysis reports, manuscript contributions, and technical assessments of documents related to BARDA's mission, such as 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 new program areas aligned with BARDA's mission.
  • Provide recommendations for project-development-level portfolio management and oversight.
  • Recommend or advise on development and improvement of Total Life Cycle Cost efforts and participate in market research.
  • Provide clinical development subject-matter expertise to BARDA's medical countermeasure programs.
  • Oversee and review clinical studies, regulatory submissions, and study-specific documents, including 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 with medicinal chemistry; preclinical development including animal models, pharmacology, and toxicology; advanced clinical development; analytical product testing and testing 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 techniques; sterile manufacturing and filling; and sterile facilities and gowning.
  • Expertise in registrational Phase II/III trials for Senior SME candidates.
  • Strong project management and clinical team leadership skills.

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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