Scientific Program Analyst

Overview
Drodex) is looking for
Scientific Program Analyst
to provide Scientific & Programmatic Assistance Services in support of the Biomedical Advanced Research and Development Authority (BARDA) within the HHS Administration for Strategic Preparedness and Response (ASPR).

These positions are part of BARDA's CORE (Critical Operations, Research & Expertise) initiative to advance the R&D of medical countermeasures (MCMs) against CBRN threats, pandemic influenza, and emerging infectious diseases.

As a Scientific Program Analyst, you'll combine technical acumen with program support expertise—helping BARDA manage complex R&D portfolios and accelerate innovation in public-health preparedness.

Location:
Hybrid (Washington, DC metro area preferred; remote flexibility available)

Responsibilities

• Support BARDA's research and development programs through data analysis, project coordination, and documentation.
• Provide advisory support on technical, regulatory, and scientific matters under senior program direction.

• Conduct advanced analytical activities, including:

• Data transfer, cleaning, integration, and validation

• Statistical modeling, visualization, and report preparation

• Draft and review Statements of Work (SOW), Performance Work Statements (PWS), Independent Government Cost Estimates (IGCE), and other acquisition documents.

• Participate on Program Coordination Teams (PCTs) and Technical Evaluation Panels (TEPs) to evaluate scientific proposals and research outcomes.
• Analyze protocols, study reports, and regulatory documentation for scientific accuracy and program alignment.
• Provide research and analytical support for Total Life Cycle Cost (TLCC) management, market research, and process improvement initiatives.
• Collaborate with BARDA staff and interagency partners to develop new MCM program areas and assess technology readiness.

Qualifications
Education:

• Master's degree or higher in biological, chemical, or physical sciences (e.g., biology, chemistry, engineering, computer science, statistics, public health, or related).
• Doctoral or professional degree preferred.

Experience / Skills

• Minimum of 8 years of relevant experience in biotechnology, pharmaceutical R&D, or government-funded research programs supporting MCM or ARD initiatives.

• Demonstrated knowledge of:

• Clinical trials, regulatory guidelines (FDA, ICH, CDISC), or CMC manufacturing processes

• Data analysis and statistical programming (SAS, R, or comparable tools)

• Quality systems, laboratory research, or public-health program evaluation

• Experience coordinating technical reviews and contributing to scientific reports or proposals.

• Excellent analytical, organizational, and communication skills.
• Ability to manage multiple projects and competing priorities in a high-impact environment.

Clearance

• Public Trust Eligible

Desired Qualifications

• PhD, MD, or equivalent advanced degree in life sciences, engineering, or related field.
• Experience working with BARDA, NIH, CDC, DoD, or similar public-health research entities.
• Background in regulatory affairs, pharmaceutical manufacturing, or Total Life Cycle Cost management.
• Strong aptitude for synthesizing complex data and advising program leadership.

About Drodex
Drodex LLC provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leave of absence, compensation, and training.