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Biomedical Engineering Consulting Jobs in Virginia

ECS

ISO Coordinator with Security Clearance

Hampton, VA · On-site

$75K - $130K/yr

Build strong relationships with scientists, engineers, contracting officers, IT professionals, and ... Knowledge of the biomedical research landscape is a plus. * Two years or more experience in Federal ...

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All JobsBiomedical Engineering Consulting JobsBiomedical Engineering Consulting Jobs in Virginia

Biomedical Engineering Consulting information

See Virginia salary details

$40.6K

$94K

$138.8K

How much do biomedical engineering consulting jobs pay per year?

As of Sep 15, 2026, the average yearly pay for biomedical engineering consulting in Virginia is $93,994.00, according to ZipRecruiter salary data. Most workers in this role earn between $73,900.00 and $115,000.00 per year, depending on experience, location, and employer.

What is biomedical engineering consulting?

Biomedical engineering consulting involves providing expert advice and solutions related to the design, development, and implementation of medical devices, healthcare technologies, and related systems. Consultants in this field help organizations navigate regulatory requirements, improve product designs, troubleshoot technical issues, and ensure compliance with industry standards. They often work with hospitals, medical device companies, and research institutions to optimize processes and bring innovative products to market safely and efficiently.

How do biomedical engineering consultants typically collaborate with clients and multidisciplinary teams during a project?

Biomedical engineering consultants frequently work alongside clients such as hospitals, medical device companies, or research institutions, as well as multidisciplinary teams including clinicians, regulatory specialists, and product designers. Effective collaboration often involves participating in regular meetings, clarifying technical requirements, and translating complex engineering concepts for non-technical stakeholders. Consultants also coordinate project timelines, ensure compliance with industry regulations, and provide ongoing technical support throughout the product development or implementation process. Building strong communication and project management skills is essential for thriving in this collaborative environment.

What are the key skills and qualifications needed to thrive as a biomedical engineering consultant, and why are they important?

To thrive as a Biomedical Engineering Consultant, you need a solid background in biomedical engineering principles, regulatory standards, and a relevant degree, often at the bachelor’s or master’s level. Familiarity with industry-standard tools such as CAD software, statistical analysis programs, and a working knowledge of medical device regulations (like FDA or ISO standards) is crucial. Strong problem-solving skills, effective communication, and the ability to collaborate with multidisciplinary teams set top consultants apart. These skills are vital to ensure innovative, compliant solutions and successful client outcomes in a complex and regulated field.

What is the difference between Biomedical Engineering Consulting vs Biomedical Equipment Technician?

AspectBiomedical Engineering ConsultingBiomedical Equipment Technician
CredentialsBiomedical engineering degree, certifications like CBET or BIETAssociate or bachelor's in biomedical technology, CBET certification
Work EnvironmentConsulting firms, hospitals, medical device companiesHospitals, clinics, service centers
Employer & IndustryConsulting firms, healthcare, medical device industryHealthcare facilities, medical equipment service providers
Job FocusDesign, development, regulatory compliance, project managementMaintenance, repair, calibration of medical equipment

While both roles involve medical devices, Biomedical Engineering Consulting focuses on design, development, and advising on medical systems, whereas Biomedical Equipment Technicians primarily handle maintenance and repair of equipment on-site.

What does a biomedical engineering consulting do?

A biomedical engineering consulting professional provides expertise in designing, evaluating, and improving medical devices, equipment, and systems. They often analyze clinical needs, ensure regulatory compliance, and apply engineering principles to develop innovative healthcare solutions, typically working with cross-disciplinary teams and utilizing tools like CAD software. Their work supports hospitals, medical device companies, and research institutions to enhance patient care and safety.

What are popular job titles related to Biomedical Engineering Consulting jobs in Virginia?

For Biomedical Engineering Consulting jobs in Virginia, the most frequently searched job titles are:

What job categories do people searching Biomedical Engineering Consulting jobs in Virginia look for?

The top searched job categories for Biomedical Engineering Consulting jobs in Virginia are:

Biomedical Engineering Consulting jobs near you
Infographic showing various Biomedical Engineering Consulting job openings in Virginia as of August 2026, with employment types broken down into 70% Full Time, 16% Part Time, and 14% Contract. Highlights an 90% In-person, 3% Hybrid, and 7% Remote job distribution, with an average salary of $93,994 per year, or $45.2 per hour.

Clinical Protocol Developer

Portsmouth, VA • Hybrid

Odyssey Systems Consulting Group, Ltd.
Public Administration • 1 - 5K employees
Learn more about Odyssey Systems Consulting Group, Ltd.external

$23.50 - $31.25/hr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 6 days ago

Job description

Odyssey is seeking a Clinical Protocol Developer to support the Clinical Investigation Department (CID) and CTRG (Combat Trauma Related Group) at the Navy Medical Center, Portsmouth (NMCP) Virginia. The mission of the command is to support the national interests of the United States by providing professional education and development, providing quality patient care, being responsive and ready for deployment, and taking care of each other as shipmates. NMCP conducts biomedical research in general surgery, psychology, otolaryngology, pediatrics, nursing research, orthopedics, women’s health, and emergency medicine, which are relevant to the Graduate Medical Education Program.

***Contingent upon contract award***


Duties include, but are not limited to:

  • Provide technical and scientific support for the development and execution of investigator-initiated protocols and clinical trials at NMCP. This position will partner with the PI to fully develop an idea from the letter of intent (LOI) stage to an ethical and IRB/IACUC-compliant protocol that can be successfully executed at NMCP.
  • Assist physicians/scientists in developing, writing and producing human and animal research protocols and nonhuman subjects’ protocols NMCP CID and GME.
  • Assist the government PIs with the preparation of new investigator-initiated trials, coordination of the submission, submission of amendments and regulatory compliance reports, and the development of the final product (presentation and/or publication), subject to final Government approval.
  • Assist with preparing informed consent statements and other study related research documents, subject to final Government approval.
  • Conduct literature reviews and draft scientific and technical documents, subject to final Government approval.
  • Assist with ensuring government PI-initiated protocols contain quality research design, and meet DOD standards for ethics and compliance, subject to final Government approval.
  • Assist with the amendment of existing investigator-initiated protocols, subject to final Government approval.
  • Assist the government PI with addressing Scientific Review Committee (SRC), Institutional Review Board (IRB), and other committee queries.
  • Assist the PI with Academic Research Competition (ARC) queries and submissions.
  • Attend and assist with the planning of committee meetings for research specific working groups to facilitate development. Contractor shall not function as a voting member.
  • Assist with administering the study development tracking system and updating protocol details and development events in eIRB system, subject to final Government approval.
  • Work with the data management team, clinical operations team and other research collaborators (as required) in transitioning projects from the development team to the operations team that incorporates the clinical details needed to treat patients and the research elements to answer study questions.
  • Assist the clinical research coordinator in the development of specimen submission. Specimen submission shall be in accordance with the Government’s protocols and are in accordance with requirements and regulations for research studies and as determined by the project leaders. Specimen submission is subject to final Government approval.
  • Assist the research and statistical data coordinators, database developers and database administrators in study database development and data monitoring planning, subject to final Government approval.
  • Assist with collecting information on reported problems regarding consistency and/or clarity in open protocols.
  • Assist with initial and follow-on updates of study registration on clinicaltrials.gov, including facilitation of Quality Assurance (QA) Review comments with coordination of the PIs, subject to final Government approval.
  • Participate in the collection of data, supporting both human and animal protocols.
  • Provide education and training to researchers and staff on protocol development within and outside department. Contractor shall not provide education and training to Government or military personnel without prior endorsement by the COR and the cognizant local Government Staff Training Manager.  All education and training materials are subject to final Government approval.

***Contingent upon contract award***


Minimum Required Qualifications:

Citizenship: Must be a US citizen.

Clearance: Ability to Obtain Secret

Education:   Masters degree in a biological, health science, physiology ,veterinary medicine, or related field.

Years of Experience:  Three years of relevant research experience.

Certifications: N/A

Additional Information

Location: 620 John Paul Jones Circle, Portsmouth, VA 23708

Travel: 10%

Remote, Onsite, or Hybrid: Onsite

#LI-JC1

***Contingent upon contract award***


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.

Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities


Final compensation for this position will be determined by various factors such as the Federal Government contract labor categories and contract wage rates, relevant work experience, specific skills and competencies, geographic location, education, and certifications.

This position is filled through continuous recruitment and will remain open until a sufficient pool of applications has been received.
Hired applicants may be eligible for benefits, including but not limited to, medical, dental, vision, life insurance, Tricare supplement, short-term disability, long-term disability, 401(k) match, flexible spending accounts, health savings accounts, employee assistance program, learning and development benefit, paid time off, and holidays.
Odyssey Benefits

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