Product Management Support - Blood Subject Matter Expert
Core
Provide specialized medical and technical expertise to the Defense Health Agency (DHA) for the development and management of blood and blood products, blood research, and combat casualty care products and devices.
Role type
Senior Product Management Support / Subject Matter Expert
Builds
Medical products, research initiatives, and combat casualty care devices for the Defense Health Agency
Domain
Defense / Healthcare / Hematology / Transfusion Medicine
Required skills
Subject matter expertise in blood products and hematology, traumatic hemorrhage, and combat casualty care, medical product development lifecycle knowledge, DoD acquisition processes, clinical trial design and execution, chemistry manufacturing and controls (CMC), market research, technical risk assessment, policy and regulation development
Preferred skills
Active DoD Secret clearance
Technologies
None explicitly listed
Responsibilities
Serve as a subject matter expert in blood and blood products, Provide technical expertise related to traumatic hemorrhage and transfusion medicine, Provide senior technical input to Product Managers and PMO leadership, Support advanced development requirements for medical products, Independently manage multiple technical efforts and projects, Participate in Integrated Product Teams and technical forums, Support product development design sessions, Conduct market research and monitor technology developments, Engage with Government, industry, academic, and clinical stakeholders, Assess and monitor technical risks, Support Product Managers with acquisition documentation throughout the DoD Acquisition Lifecycle, Provide technical input to Acquisition Strategies and Requirements Documents, Prepare white papers, RFI responses, and executive summaries, Review program documentation for technical accuracy, Provide technical input related to non-clinical studies and clinical trial design, Review regulatory applications and clinical protocols, Provide technical input concerning CMC for biologics and devices, Support development of plans for testing, fielding, and training, Support development and implementation of policies and regulations, Review FDA recommendations and clinical documentation, Communicate complex technical information to multiple organizational levels
Seniority
Senior, hands-on IC
