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Biomedical Signal Processing Jobs in Washington (NOW HIRING)

mPower, Inc.

Scientific Program Manager

Bethesda, MD · On-site

D., M.D., or equivalent) in neuroscience, neurobiology, neurology, biomedical sciences, or a ... Familiarity with federal advisory committee processes, scientific workshops, and public-private ...

mPower, Inc.

Scientific Program Manager

Bethesda, MD · On-site

D., M.D., or equivalent) in neuroscience, neurobiology, neurology, biomedical sciences, or a ... Familiarity with federal advisory committee processes, scientific workshops, and public-private ...

mPower, Inc.

Senior Grants Policy Analyst

Bethesda, MD · On-site

Strategic Analysis • Evaluate grants administration processes and identify opportunities for ... signals in application materials based on available information. These tools assist our recruitment ...

mPower, Inc.

Program Coordinator

Bethesda, MD

$65K - $80K/yr

... process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available ...

mPower, Inc.

Program Coordinator

Bethesda, MD · On-site

$65K - $80K/yr

Master's degree in a scientific discipline, such as bioengineering, biomedical/chemical/materials ... If you would like more information about how your data is processed, please contact us.

mPower, Inc.

Program Coordinator

Bethesda, MD · On-site

Master's degree in a scientific discipline, such as bioengineering, biomedical/chemical/materials ... If you would like more information about how your data is processed, please contact us.

iNovex Information Systems

System Engineer 1

Annapolis, MD · On-site

$73K - $109K/yr

Aeronautics, Biomedical, Chemical, Civil, Computer, Electrical, Environmental, Mechanical, Nuclear ... Familiar with RF tools (network analyzers, signal generators, spectrum analyzers, oscilloscopes ...

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Biomedical Signal Processing information

See Washington salary details

$17

$32

$44

How much do biomedical signal processing jobs pay per hour?

As of Jun 29, 2026, the average hourly pay for biomedical signal processing in Washington is $32.31, according to ZipRecruiter salary data. Most workers in this role earn between $27.50 and $36.49 per hour, depending on experience, location, and employer.

What are some typical daily responsibilities for someone working in Biomedical Signal Processing?

Professionals in Biomedical Signal Processing often spend their days analyzing physiological signals such as EEGs, ECGs, or EMGs, designing algorithms to interpret data, and validating systems to ensure accuracy and reliability. They collaborate closely with clinicians, researchers, and software developers to translate clinical needs into effective technical solutions. Tasks may also include testing prototypes, troubleshooting data acquisition systems, and preparing reports or research publications. This role can be a mix of independent analytical work and cross-functional teamwork, offering both technical and collaborative challenges.

What is the highest paying biomedical job?

In biomedical signal processing, senior roles such as biomedical engineering managers or lead researchers tend to have the highest salaries, often exceeding six figures. These positions typically require advanced degrees, extensive experience, and expertise in areas like medical device development, data analysis, and regulatory compliance.

What is the salary of a biomedical signal processing engineer?

The salary of a biomedical signal processing engineer typically ranges from $70,000 to $120,000 annually, depending on experience, education, location, and industry. Entry-level positions may start lower, while experienced professionals or those in specialized roles can earn higher salaries, especially with advanced skills in signal analysis and programming tools like MATLAB or Python.

Does signal processing pay well?

Biomedical signal processing is a specialized field that often offers competitive salaries, especially for those with advanced degrees and skills in algorithms, programming, and data analysis. Salaries can vary based on experience, location, and industry, with roles in healthcare, research, and technology typically providing higher compensation.

What are the key skills and qualifications needed to thrive in the Biomedical Signal Processing position, and why are they important?

To thrive in Biomedical Signal Processing, you need a solid background in biomedical engineering, signal analysis, and quantitative methods, typically supported by a relevant degree or advanced coursework. Familiarity with MATLAB, Python, LabVIEW, and signal processing toolboxes, as well as knowledge of regulatory standards like FDA or ISO, is essential. Critical thinking, attention to detail, and strong communication skills help professionals collaborate effectively with multidisciplinary teams. These competencies are crucial for developing accurate, reliable solutions that support patient care and medical research.

What is a Biomedical Signal Processing job?

A Biomedical Signal Processing job involves analyzing physiological signals, such as ECG, EEG, and EMG, to extract meaningful information for medical diagnosis, treatment, and research. Professionals in this field use mathematical models, algorithms, and machine learning techniques to improve healthcare technologies. They work in hospitals, research institutions, medical device companies, and academia to develop and optimize signal processing methods for clinical applications.

Are bioengineers paid well?

Biomedical signal processing is a specialized field within biomedical engineering, and professionals in this area typically earn competitive salaries that reflect their technical skills and education. Entry-level positions often start with moderate pay, while experienced engineers with advanced certifications can earn higher salaries, especially in research, development, or clinical environments.
What are popular job titles related to Biomedical Signal Processing jobs in Washington? For Biomedical Signal Processing jobs in Washington, the most frequently searched job titles are:
What job categories do people searching Biomedical Signal Processing jobs in Washington look for? The top searched job categories for Biomedical Signal Processing jobs in Washington are:
Biomedical Signal Processing jobs near you
Infographic showing various Biomedical Signal Processing job openings in Washington as of June 2026, with employment types broken down into 1% Internship, 65% Full Time, 9% Part Time, and 25% Contract. Highlights an 88% Physical, 2% Hybrid, and 10% Remote job distribution, with an average salary of $67,200 per year, or $32.3 per hour.

Scientific Program Manager (Pharmacovigilance)

Nextonic Solutions LLC

Bethesda, MD

Full-time

Posted 9 days ago

Key responsibilities

  • Oversee operational aspects of the VRC Clinical Trials Program Pharmacovigilance Team, including safety signal management activities and ensuring the detection, assessment, understanding, and prevention of safety events for each investigational product.

  • Create and adapt drug safety and pharmacovigilance procedures based on domestic and international regulations and VRC/NIAID policies and procedures.

  • Review safety events for completeness and trends, analyze comprehensive safety data with the PV team, and communicate findings according to PV Teamwork instructions, SOPs, and plans.

Job description

Nextonic Solutions is seeking a highly ambitious, adaptable, structured, and detail-oriented Scientific Program Manager to join our vibrant team at the National Institutes of Health (NIH), Vaccine Research Center (VRC), Clinical Trials Program (CTP).

Requirements: 

-Oversee operational aspects of the VRC Clinical Trials Program (CTP) Pharmacovigilance (PV) Team, which leads the process for safety signal management activities, and ensures the detection, assessment, understanding and prevention of safety events for each investigational product (IP) the VRC manufactures for clinical research.

-Support tactical organization, planning and development for the VRC CTP PV Team as led by CTP Leadership.

-Create and adapt drug safety and pharmacovigilance procedures based on prevailing domestic and international regulations and VRC/NIAID policies and procedures.

-Review safety events for completeness and trends; analyze comprehensive safety data in consultation with PV team; communicate findings per PV Teamwork instructions, SOPs and plans.

-Participate on cross functional, multidisciplinary teams within the CTP/VRC and with external collaborators to plan for regulatory submissions, discuss safety signals and review aggregate safety data.

-Draft, review and finalize PV data sharing agreements with collaborators who receive VRC manufactured investigational products. Ensure timely receipt of PV agreement deliverables.

-Work with VRC’s external partners to gather PV information/data and review it utilizing the PV data system platform (ARGUS).

-Author and provide strategic input and oversight for PV-related sections of periodic regulatory documents (i.e., IND annual reports, DSURs, IB updates) according to the agreed process and timelines.

-Monitor and evaluate safety profiles of VRC manufactured investigational products to detect any change in risk profile.

-Collaborate with CTP protocol operations, clinical and quality and risk management teams, as well as the VRC Regulatory and Strategic Planning groups, to ensure coordinated and effective risk mitigation strategies throughout the product lifecycle.

-Perform QC checks of PV Team documents and document repository to ensure completeness and accuracy.

-Assign projects and set deadlines for PV Team staff and facilitate PV team meetings.

-Maintain knowledge of vaccine and monoclonal antibody safety profiles and product development status; review relevant biomedical literature or other scientific data. 

-Communicate effectively, professionally, and cordially with internal team members and external collaborators with clear, concise, and timely written and verbal communication and presentations.

-Complete and follow up on all assigned tasks in a timely and professional manner.

-Attend all team meetings as requested with punctuality and preparedness.


Qualifications: 

-Clinical Advanced degree (NP, PA, MD, DO, etc.) strongly preferred.

-Minimum 5 + years’ experience in PV or relevant clinical trials experience with significant experience in preparing safety summaries for regulatory documents in a biotechnology, pharmaceutical company, government, or CRO environment.

-Knowledge of clinical trial, drug safety and PV methodologies including safety profile and risk/benefit analysis; detailed comprehension of global regulatory requirements in PV is a plus.

-Experience with MedDRA and drug coding reviews.

-Experience in the conduct and management of clinical trials, phase I – III vaccine or monoclonal antibody clinical trials preferred.

-Strong background in clinical trial drug safety is required.

-An understanding of medical terminology and ability to summarize medical information is required.

-Team lead experience is preferred.

-Strong attention to detail and follow-up skills is required.

-Must be flexible and willing to take on administrative responsibilities to support the PV team, including drafting meeting agendas and note taking, filing documents, scheduling meetings, sending, and tracking requests and reminders to collaborators for data collection.

-Must be proactive and able to create contingency plans to deal with possible challenges and roadblocks.

-Excellent computer and database skills, familiarity with ARGUS platform is preferred.

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