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Institutional Review Board Jobs in Silver Spring, MD

Goodwin Living

Nurse Practitioner

Alexandria, VA · On-site

  • Medical

  • PTO

Is an active member of the Goodwin House Institutional Review Board. * Plans and facilitates health education programs for residents. Provides education to residents on health related matters via a ...

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All JobsInstitutional Review Board JobsInstitutional Review Board Jobs in Silver Spring, MD

Institutional Review Board information

See Silver Spring, MD salary details

$52.8K

$86.7K

$138.3K

How much do institutional review board jobs pay per year?

As of Aug 19, 2026, the average yearly pay for institutional review board in Silver Spring, MD is $86,705.00, according to ZipRecruiter salary data. Most workers in this role earn between $70,400.00 and $102,000.00 per year, depending on experience, location, and employer.

What does an institutional review board professional do?

An IRB professional is responsible for reviewing research studies involving human subjects to ensure they meet ethical and regulatory standards. They assess protocols for compliance with federal, state, and institutional guidelines to protect participant rights and welfare. Their duties include reviewing applications, providing guidance to researchers, and ensuring informed consent processes are properly implemented. IRB professionals often work in universities, hospitals, or research institutions.

What are the key skills and qualifications needed to thrive in an institutional review board position?

To thrive as an Institutional Review Board (IRB) member or administrator, you need a strong understanding of research ethics, federal regulations, and compliance requirements, often supported by a background in health sciences, law, or ethics. Familiarity with electronic IRB management systems, regulatory databases, and training in human subjects research protection (such as CITI certification) is typically required. Attention to detail, critical thinking, and the ability to communicate diplomatically with diverse stakeholders are crucial soft skills. These abilities are essential to ensure the ethical review and approval of research projects, safeguarding participants and maintaining institutional integrity.

What are some typical challenges faced by professionals working on an institutional review board?

Professionals working on an Institutional Review Board often navigate the complex balance between facilitating innovative research and upholding strict ethical standards to protect human subjects. One common challenge is keeping current with frequently evolving regulations and interpreting how they apply to a wide range of research proposals. IRB members must also manage high volumes of submissions and coordinate with researchers, legal advisors, and compliance officers to resolve issues promptly. This role requires continuous professional development and a collaborative approach to problem-solving in a multidisciplinary setting.

How to become an institutional review board reviewer?

To become an institutional review board (IRB) reviewer, individuals typically need relevant experience in research ethics, healthcare, or scientific fields, along with familiarity with federal regulations such as the Common Rule. Many IRB members have advanced degrees and may complete training programs on human subjects research protections. Active participation often requires being part of an institution that has an IRB and attending regular meetings to review research protocols.

How to get an Institutional Review Board job?

To work as an Institutional Review Board (IRB) member or staff, candidates typically need a background in research, ethics, or healthcare, along with knowledge of federal regulations such as the Common Rule. Relevant experience, professional certifications, and understanding of human subjects protection are often required, and positions may require a bachelor's or advanced degree. Training on IRB procedures and compliance is also beneficial for securing such roles.

What are popular job titles related to Institutional Review Board jobs in Silver Spring, MD?

For Institutional Review Board jobs in Silver Spring, MD, the most frequently searched job titles are:

What job categories do people searching Institutional Review Board jobs in Silver Spring, MD look for?

The top searched job categories for Institutional Review Board jobs in Silver Spring, MD are:

Institutional Review Board jobs near you
Infographic showing various Institutional Review Board job openings in Silver Spring, MD as of August 2026, with employment types broken down into 75% Full Time, and 25% Contract. Highlights an 75% In-person, and 25% Remote job distribution, with an average salary of $86,705 per year, or $41.7 per hour.

Senior Medical Officer

Veritas Management Group (VMG)

Rockville, MD • On-site

$180 - $240/hr

Other

Posted 13 days ago

Job description

Position Title: Senior Medical Officer, Full-Time
Contract Duration: 12-month base period with renewable option periods
Location: Rockville, Maryland
Department: Veritas Management Group/NIH SOAR

Summary

Veritas Management Group (VMG) is a leading management consulting firm offering solutions to complex challenges involving public health, technology, and military domains. We serve government and commercial sector organizations, academic institutions, and non-profit organizations, domestically and globally. We are committed to transforming public health through equitable, data-driven solutions.

VMG is seeking an experienced Senior Medical Officer to support the National Institute of Allergy and Infectious Diseases (NIAID), Division of Microbiology and Infectious Diseases (DMID). This position provides senior medical leadership and scientific oversight for DMID-sponsored clinical research programs by advising on Institutional Review Board (IRB) processes, pediatric clinical care, hospital pharmacy practices, clinical trial oversight, protocol review, and participant safety. The Senior Medical Officer will collaborate with federal staff, investigators, regulatory agencies, sponsors, and academic partners to support the safe and effective execution of infectious disease clinical trials.

Key Responsibilities
  • Provide medical expertise and recommendations regarding Institutional Review Board (IRB) processes and clinical research oversight.
  • Advise DMID staff on pediatric clinical care and hospital pharmacy practices related to clinical research.
  • Provide guidance on the oversight and administration of clinical trials.
  • Review clinical trial protocols and provide recommendations to improve study quality, participant safety, and operational effectiveness.
  • Evaluate safety and operational issues associated with DMID-sponsored clinical research protocols.
  • Assess Serious Adverse Events (SAEs) reported during clinical trials and provide medical recommendations.
  • Review and provide recommendations regarding the design and safety of clinical trials.
  • Represent DMID in communications with the U.S. Food and Drug Administration (FDA), study sponsors, and academic partners regarding clinical trial design and safety.
  • Review safety reports and serve as a medical safety expert on safety committees.
  • Participate in Office of Clinical Research Affairs (OCRA) meetings, training sessions, and safety-related educational programs.
  • Develop policies and guidelines that support the care and protection of patients enrolled in DMID-sponsored clinical studies.
  • Prepare written reports, medical reviews, recommendations, and other technical documents supporting clinical research activities.
  • Collaborate with multidisciplinary research teams to ensure compliance with NIH policies, federal regulations, and Good Clinical Practice (GCP) standards.
  • Provide expert medical consultation to investigators, federal leadership, and research partners on complex clinical and regulatory issues.
Required Qualifications
  • Medical Degree (M.D. or D.O.) from an accredited medical school.
  • Minimum of ten (10) years of professional medical experience in clinical medicine, clinical research, or a related healthcare field.
  • Experience supporting clinical trial oversight and protocol review.
  • Experience assessing clinical safety issues and Serious Adverse Events (SAEs).
  • Knowledge of Institutional Review Board (IRB) processes, FDA regulations, and Good Clinical Practice (GCP).
  • Experience providing medical consultation for multidisciplinary clinical research programs.
  • Superior medical writing skills.
  • Excellent oral and written communication skills.
  • Proficiency with Microsoft Office Suite.
Preferred Qualifications
  • Board certification in a relevant medical specialty.
  • Experience supporting NIH, NIAID, or other federally funded clinical research programs.
  • Experience in pediatric clinical care or pediatric clinical research.
  • Experience supporting infectious disease clinical trials.
  • Experience serving on clinical safety committees or similar oversight groups.
  • Experience developing clinical policies, practice guidelines, and research procedures.
  • Experience working with FDA-regulated clinical research and sponsor communications.
Work Environment
  • Full-time position (40 hours per week).
  • Monday through Friday schedule.
  • Position is located at the National Institute of Allergy and Infectious Diseases (NIAID), Division of Microbiology and Infectious Diseases (DMID) in Rockville, Maryland.
  • Telework is not available.
  • Professional office environment supporting clinical research oversight and medical program administration.
  • Position requires close collaboration with physicians, investigators, federal program officials, regulatory agencies, sponsors, academic partners, and multidisciplinary scientific teams.
  • No direct patient care responsibilities.
  • No security clearance required.
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