Research Product Manager Jobs in Washington, DC
Research Product Manager jobs in Washington, District of Columbia are in strong demand, concentrated in the Capitol Hill corridor, Foggy Bottom, and the NoMa innovation district across federal contracting, policy research, health informatics, and defense technology. Employers hiring right now include Children's National Hospital, Georgetown University, and Howard University. Find a role that fits below and apply directly.
Find Research Product Manager JobsOverview
Open roles139+
Top employerChildren's National Hospital
Work type49% On-site
Top credentialBachelor's degree
Companies hiring73
Showing 5 of 139+ Research Product Manager jobs
Clinical Research Coordinator II - Oncology
We won't show you this job again
New 1m ago
MedStar Health
Clinical Research Coordinator II - Oncology
Washington, District of Columbia
New 1m ago
STINGRAI Tech Advisor (Operations Research Analyst 4)
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New 1m ago
HII
STINGRAI Tech Advisor (Operations Research Analyst 4)
Washington, District of Columbia
New 1m ago
Temporary Research Assistant
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New 1m ago
Georgetown University
Temporary Research Assistant
Washington, District of Columbia
New 1m ago
Research Assistant (Edwin O. Reischauer Center for East Asian Studies)
We won't show you this job again
New 1m ago
Johns Hopkins University
Research Assistant (Edwin O. Reischauer Center for East Asian Studies)
Washington, District of Columbia
New 1m ago
Director, Research Advisory Services
We won't show you this job again
New 1m ago
EAB
Director, Research Advisory Services
Washington, District of Columbia
New 1m ago
New 1m ago
Clinical Research Coordinator II - Oncology
MedStar Health·Washington, District of Columbia
Job functions:
Bachelor's degree
10,000+ employees
Job Description
About this Job:
General Summary of Position
Implements and coordinates research and administrative procedures for the successful management of clinical trials. Performs diverse administrative duties requiring analysis sound judgment and a high level of knowledge of study specific protocols. Enters study and/or research participant data into the Clinical Trial Management System (CTMS) as applicable.
Implements and coordinates research and administrative procedures for the successful management of clinical trials. Performs diverse administrative duties requiring analysis sound judgment and a high level of knowledge of study specific protocols. Enters study and/or research participant data into the Clinical Trial Management System (CTMS) as applicable.
Primary Duties and Responsibilities
- Regulatory responsibilities include the oversight and/or responsibility for the Intuitional Review Board (IRB) submissions and other related regulatory forms (e.g. scientific review) and adhering to the timelines of the study start-up process; developing informed consent documents and other documents as applicable; supporting the safety of clinical research participants; ensureing the appropriate delegation of study related tasks (i.e. Delegation of Authority).
- Explains the informed consent process and the study to the research participant (e.g. purpose duration risks/benefits) and obtains all required signatures; ensures the research participant has sufficient time and opportunity to ask the investigator medical questions; documents the informed consent process in the source document and provides the research participant with a copy of the informed consent.
- Develops an effective recruitment plan (e.g. central recruitment core); recruits research participants and discuss study protocol; educates research participants about protocol expectations and meets with research participants for each visit and maintains accessibility to discuss any questions or concerns regarding the study;
- Oversees the development of advertising materials; participates in teleconferences and/or meetings to review study progress and conduct.
- Data entry responsibilities include the completion and maintenance of case report forms and reviews data against the research participant's medical record for completeness and accuracy; addressing all queries clarifications and outstanding data queries and appropriately communicating with the sponsor and/or Contract Research Organization (CRO); completing and submitting case report forms on as close to a real time basis as possible.
- Ensures proper collection processing and shipment of biospecimens and pharmacokinetics as applicable (e.g. centrifuge freezing refrigeration) and maintains current Occupational Safety and Health Administration (OSHA) training regarding Bloodborne Pathogens;
- Assists with maintaining equipment (e.g. calibration preventive maintenance); communicates with manager investigator and sponsor regarding abnormal laboratory values; maintains Internal Air and Transportation Association (IATA) training for routine packaging labeling and transporting of biological materials.
- Study conduct responsibilities include research participant interviews and assessments at study visits as required by protocol; assessing and ensuring research participant safety through study participation; maintaining close communication with investigator;
- Attending investigator meetings as appropriate and communicating relevant information to the research team; understanding and proficiently communicating all components of research documents such as protocol investigator brochure and research instructions.
- Receives and maintains test articles from sponsor and inventory test articles; works with research pharmacist as applicable; stores test article supplies according to Food and Drug Administration (FDA) regulations and sponsor requirements; administers test article as appropriate;
- Retrieves test articles and calculates research participant compliance; maintains randomization and emergency codes of test article; documents on accountability log and research participant record (e.g. test article received used disposed).
- Ensures that non-serious and serious adverse events are properly identified documented and reported according to all applicable requirements; presents investigator with relevant information for determination of seriousness causality and intervention; acts on investigator's recommendation for adverse event intervention (e.g. stop test article call research participant re-test treat); maintains follow-up to determine resolution of adverse event.
- Understands and complies with rules for billing Medicare Medicaid and third party payors for services drugs devices tests and procedures rendered in the clinical research context;
- Responsible for reviewing understanding and accepting the billing matrix/billing plan generated by administration for research participants enrolled in clinical studies; ensures research participant stipends have been routed in a timely manner as applicable.
- Study close-out responsibilities include return or disposition of unused supplies per sponsors requirement; reconciling test article accountability; document research participants who are lost to follow-up or who have dropped out (e.g. causes contact efforts); ensuring long term storage of documents; submitting IRB closing report (i.e. termination) after sponsor has closed study site.
- Acts as a liaison with research participants investigators sponsors and healthcare professionals; prepares for site qualification study initiation monitoring and close-out visits;
- Ensures all research participant encounters are updated as appropriate and within one business day in clinical trial management system (CTMS); works effectively with multidisciplinary ancillary and inter-professional research teams; possesses a basic understanding of scientific center goals and the importance of serving our customers.
Minimal Qualifications
Education
Education
- Bachelor's degree or an allied health or related professional degree required, or equivalent work experience
Experience
- 2 years of relevant clinical research experience required
- Experience in a healthcare setting preferred
- Undergraduate and/or work experiences that demonstrates aptitude for research facilitation preferred
Knowledge Skills and Abilities
- Verbal and written communication skills.
- Basic computer skills preferred.
MedStar Health
Clinical Research Coordinator II - Oncology
Washington, District of Columbia
New 1m ago10,000+ employees
Job functions:
Bachelor's degree
Job Description
About this Job:
General Summary of Position
Implements and coordinates research and administrative procedures for the successful management of clinical trials. Performs diverse administrative duties requiring analysis sound judgment and a high level of knowledge of study specific protocols. Enters study and/or research participant data into the Clinical Trial Management System (CTMS) as applicable.
Implements and coordinates research and administrative procedures for the successful management of clinical trials. Performs diverse administrative duties requiring analysis sound judgment and a high level of knowledge of study specific protocols. Enters study and/or research participant data into the Clinical Trial Management System (CTMS) as applicable.
Primary Duties and Responsibilities
- Regulatory responsibilities include the oversight and/or responsibility for the Intuitional Review Board (IRB) submissions and other related regulatory forms (e.g. scientific review) and adhering to the timelines of the study start-up process; developing informed consent documents and other documents as applicable; supporting the safety of clinical research participants; ensureing the appropriate delegation of study related tasks (i.e. Delegation of Authority).
- Explains the informed consent process and the study to the research participant (e.g. purpose duration risks/benefits) and obtains all required signatures; ensures the research participant has sufficient time and opportunity to ask the investigator medical questions; documents the informed consent process in the source document and provides the research participant with a copy of the informed consent.
- Develops an effective recruitment plan (e.g. central recruitment core); recruits research participants and discuss study protocol; educates research participants about protocol expectations and meets with research participants for each visit and maintains accessibility to discuss any questions or concerns regarding the study;
- Oversees the development of advertising materials; participates in teleconferences and/or meetings to review study progress and conduct.
- Data entry responsibilities include the completion and maintenance of case report forms and reviews data against the research participant's medical record for completeness and accuracy; addressing all queries clarifications and outstanding data queries and appropriately communicating with the sponsor and/or Contract Research Organization (CRO); completing and submitting case report forms on as close to a real time basis as possible.
- Ensures proper collection processing and shipment of biospecimens and pharmacokinetics as applicable (e.g. centrifuge freezing refrigeration) and maintains current Occupational Safety and Health Administration (OSHA) training regarding Bloodborne Pathogens;
- Assists with maintaining equipment (e.g. calibration preventive maintenance); communicates with manager investigator and sponsor regarding abnormal laboratory values; maintains Internal Air and Transportation Association (IATA) training for routine packaging labeling and transporting of biological materials.
- Study conduct responsibilities include research participant interviews and assessments at study visits as required by protocol; assessing and ensuring research participant safety through study participation; maintaining close communication with investigator;
- Attending investigator meetings as appropriate and communicating relevant information to the research team; understanding and proficiently communicating all components of research documents such as protocol investigator brochure and research instructions.
- Receives and maintains test articles from sponsor and inventory test articles; works with research pharmacist as applicable; stores test article supplies according to Food and Drug Administration (FDA) regulations and sponsor requirements; administers test article as appropriate;
- Retrieves test articles and calculates research participant compliance; maintains randomization and emergency codes of test article; documents on accountability log and research participant record (e.g. test article received used disposed).
- Ensures that non-serious and serious adverse events are properly identified documented and reported according to all applicable requirements; presents investigator with relevant information for determination of seriousness causality and intervention; acts on investigator's recommendation for adverse event intervention (e.g. stop test article call research participant re-test treat); maintains follow-up to determine resolution of adverse event.
- Understands and complies with rules for billing Medicare Medicaid and third party payors for services drugs devices tests and procedures rendered in the clinical research context;
- Responsible for reviewing understanding and accepting the billing matrix/billing plan generated by administration for research participants enrolled in clinical studies; ensures research participant stipends have been routed in a timely manner as applicable.
- Study close-out responsibilities include return or disposition of unused supplies per sponsors requirement; reconciling test article accountability; document research participants who are lost to follow-up or who have dropped out (e.g. causes contact efforts); ensuring long term storage of documents; submitting IRB closing report (i.e. termination) after sponsor has closed study site.
- Acts as a liaison with research participants investigators sponsors and healthcare professionals; prepares for site qualification study initiation monitoring and close-out visits;
- Ensures all research participant encounters are updated as appropriate and within one business day in clinical trial management system (CTMS); works effectively with multidisciplinary ancillary and inter-professional research teams; possesses a basic understanding of scientific center goals and the importance of serving our customers.
Minimal Qualifications
Education
Education
- Bachelor's degree or an allied health or related professional degree required, or equivalent work experience
Experience
- 2 years of relevant clinical research experience required
- Experience in a healthcare setting preferred
- Undergraduate and/or work experiences that demonstrates aptitude for research facilitation preferred
Knowledge Skills and Abilities
- Verbal and written communication skills.
- Basic computer skills preferred.
See All 139+ Research Product Manager Jobs in Washington
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Find Research Product Manager JobsResearch Product Manager Job Market in Washington
Who's Hiring
- Children's National Hospital23
- Georgetown University9
- Howard University7
- Johns Hopkins University7
- Council On Foreign Relations5
Top Industries Hiring
- Healthcare & Medical Services26
- Education19
- Technology & Software5
- Consulting & Professional Services5
- Science & Research3
Research Product Manager Jobs in Washington: Frequently Asked Questions
How do I get a research product manager job in Washington?
Focus on Washington's dominant hiring sectors: federal agencies and their contractors, health policy and public health organizations, defense and intelligence technology firms, and think tanks. Jobs concentrate in NoMa, Foggy Bottom, and the K Street corridor. Candidates with experience translating research insights into product decisions, working with cross-functional government or policy teams, and managing stakeholder-heavy roadmaps hold a clear edge in this market.
Which companies hire research product managers in Washington?
Employers hiring research product managers in Washington right now include Children's National Hospital, Georgetown University, and Howard University, based on current listings on Migrate Mate as of July 2026. Washington's market skews heavily toward federal contractors, health and policy research organizations, and defense technology firms, making it one of the most research-driven product management markets in the country.
Are there remote research product manager jobs in Washington?
Yes, though availability depends on the role's hands-on requirements. Research product management work is analytical and collaborative enough that remote and hybrid arrangements are fairly common. About 51% of research product manager openings tied to Washington are remote or hybrid as of July 2026, with remote options most prevalent in data strategy, user research synthesis, and roadmap planning roles rather than those requiring frequent agency or lab presence.
How can I get a research product manager job in Washington with little or no experience?
The most realistic entry path in Washington is through federal contractor internships or junior research analyst roles at health policy organizations, think tanks, or defense technology firms. Look for associate product manager or research coordinator titles at organizations based in NoMa or Foggy Bottom. Demonstrating familiarity with government procurement cycles, public health data platforms, or policy-driven research workflows gives entry-level candidates a meaningful advantage over generalist applicants.
Which industries hire the most research product managers in Washington?
Most research product manager openings in Washington sit in Healthcare & Medical Services, Education, and Technology & Software, per current listings on Migrate Mate as of July 2026. Washington's concentration of federal agencies, defense contractors, and public health institutions creates sustained demand for product managers who can bridge rigorous research processes with mission-driven product development.
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