Drug Development SME

Key Role:

Work with clients and internal colleagues in the development and testing of medical countermeasures for biothreat agents. Perform independent quantitative and qualitative data collection and analyses to derive insights on client issues, evaluate trends, and assess potential solutions. Develop and lead communications of practical solutions to clients in the form of data-driven presentations, briefings, and reports. Report meetings highlights and analysis products to a wide variety of audiences.

Basic Qualifications:

-6+ years of experience with leading research and development as a program manager
-3+ years of experience with drug development

-Knowledge of FDA regulatory procedures

-Ability to work in a team-based or project environment

-Ability to obtain a security clearance

-BA or BS degree in a scientific field

Additional Qualifications:

-1+ years of experience with clinical trials

-1+ years of experience with the health or medical product industries, including R&D, clinical, regulatory, marketing, strategy, operations, manufacturing, or consulting

-1+ years of experience with strategy or management consulting

-Experience with DoD acquisition processes

-Experience with infectious disease biology

-Possession of excellent analytical skills

-Possession of excellent oral and written communication skills

-Secret clearance preferred

-MA or MS degree in Life Science or Engineering preferred

-Project Management Professional (PMP) Certification


Applicants selected will be subject to a security investigation and may need to meet eligibility requirements for access to classified information.

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