Odyssey Systems

Senior Product Management Support (Force Health Protection)

Odyssey Systems$110K — $130K *
Pharmaceuticals & Biotech
8 - 10 years of experience
Job Overview by Ladders

Qualifications

  • US citizenship required.
  • Must be able to obtain NACI clearance.
  • Bachelor's degree in a scientific or health-related field required.
  • Minimum 8 years of experience in clinical/FDA regulatory product development.
  • Proficient in cGCP, cGLP, and cGMP regulations.

Responsibilities

  • Develop and organize training for GCP compliance for staff.
  • Coordinate clinical protocols and ensure FDA/DoD compliance.
  • Collaborate with DHA for IND protocol regulatory requirements.
  • Manage storage and product release for IND products.
  • Review technical documents and recommend improvements.

Benefits

  • Company-provided training opportunities.
  • Support for professional certification and growth.
  • Opportunities to work with leading healthcare regulations.
  • Contributions to impactful health-oriented projects.
  • Potential for career advancement within the organization.
Full Job Description
Position Summary

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

Duties include, but are not limited to:
  • 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***

Qualifications

Minimum Required Qualifications:

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).

Preferred Qualifications:

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.

Experience with DHA/USAMMDA preferred

Location: Defense Health Agency (DHA), 1430 Veterans Drive, Fort Detrick, MD 21702

Travel: 10%

Remote, Onsite, or Hybrid: Onsite

#LI-JC1

***Contingent upon contract award***

Odyssey Benefits

About Odyssey Systems

Odyssey Systems is an information technology company based in Rockville, Maryland. It was founded in 1997 and provides a range of IT services to government agencies and private sector clients. Odyssey Systems specializes in software development, data analytics, and cybersecurity. The company has a team of over 500 employees and has worked with clients such as the Department of Defense, the Department of Homeland Security, and the National Institutes of Health. Odyssey Systems is committed to providing innovative solutions to its clients and helping them achieve their goals.
Learn more about Odyssey Systems
Size
500 employees
Industry
Founded
1997
Revenue
$100 million

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