Senior Product Management Support (Force Health Protection) at Careers in US-MD-Frederick
- Company: Careers
- Location: US-MD-Frederick
- Posted: Sep 18, 2026
- Type: Full Time
- Salary: USD $80,000.00/Yr. - USD $170,000.00/Yr.
- Experience: 8+ years
Overview
Odyssey is looking for a a Senior Product Management Support for Force Health Protection (FHP ), to support the Defense Health Agency (DHA), at Ft. Detrick, MD. This role provides vital oversight of product management and clinical protocol accountability. It also manages Investigational New Drug (IN…
Job description
- Odyssey is looking for a a Senior Product Management Support for Force Health Protection (FHP ), to support the Defense Health Agency (DHA), at Ft. Detrick, MD. This role provides vital oversight of product management and clinical protocol accountability. It also manages Investigational New Drug (IND) products, ensures adherence to Good Clinical Practices (GCP), and coordinates with the FDA to support the clinical development of therapeutics and diagnostics.
- ***Contingent upon contract award***
Responsibilities
- Develop regulatory documentation, organize, and provide annual and refresher Good Clinical Practices (GCP) training to medical and laboratory staff.
- Coordinate the management of clinical protocols, therapeutics, prophylactics, and diagnostics, ensuring compliance with FDA and DoD regulations.
- Work with the DHA Office of Regulated Activities to ensure IND protocols meet all regulatory requirements and support submissions to the FDA and Institutional Review Boards (IRB).
- Provide storage, protocol management, and oversee product release for FHP IND products.
- Review and analyze technical documents, making recommendations to ensure sound scientific processes are used in support of investigational products.
- ***Contingent upon contract award***
Requirements
- Citizenship: Must be a US citizen.
- Clearance : Ability to Obtain NACI.
- Education: Bachelor's Degree in a scientific, health, or related field.
- Years of Experience: At least 8 years of full-time work experience in clinical/FDA regulatory product development.
- Certifications: Demonstrated experience and knowledge of Current Good Clinical Practice (cGCP), Current Good Laboratory Practices (cGLP), and Current Good Manufacturing Practices (cGMP).
- Education: Advanced degree in a scientific or health-related discipline.
- Years of experience: Extensive experience managing IND protocols and interacting with the FDA and IRBs.
- Location: Defense Health Agency (DHA), 1430 Veterans Drive, Fort Detrick, MD 21702
- Travel: 10%
- Remote, Onsite, or Hybrid: Onsite
- ***Contingent upon contract award***
Skills
Preferred
- Experience managing IND protocols
- Experience with DHA/USAMMDA
About Careers
Odyssey is a world-class technical, engineering, and integration company serving the warfighting ecosystem with airborne integration, ISR, C2, and warfighter readiness capabilities. Odyssey meets the military’s operational needs by integrating layered defense systems from equipment, technology, and services to data, information, and business operations. We streamline defense acquisition and sustainment, engineering the technical battlefield with domain-specific proficiency to ensure lethality. Odyssey is dedicated to excellent contract execution, peak organizational performance, and fostering a workplace built on employee care. Odyssey is proud to live out our core values of commitment, ambition, and respect in our work and communities through OdysseyCares , a philanthropic group focused on giving back through direct donations, an employer match program, and volunteering events.