Clinical Research Jobs in District of Columbia
Clinical Research jobs in District of Columbia are among the most active in the nation, concentrated in federal health agencies, academic medical centers, and nonprofit research institutions that define the region's life sciences ecosystem, with openings at every level from entry-level coordinator to principal investigator. The heaviest hiring is in and around Washington, D.C., Bethesda, and Silver Spring, where organizations like the National Institutes of Health, MedStar Health, and George Washington University Hospital maintain a consistent demand for clinical research professionals. Regulatory affairs, oncology trials, and NIH-funded study coordination are the most in-demand specialties right now. See the openings below and apply to the ones that match your experience.
Find Clinical Research JobsOverview
Showing 5 of 27+ Clinical Research jobs
ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.
As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.
The Sr. Clinical Research Associate (Sr. CRA) will be responsible for performing investigative site management and monitoring activities throughout the clinical trial lifecycle. This Sr. CRA role will support the client's Oncology clinical trials to ensure data integrity, subject safety, and inspection readiness at the clinical investigative sites.
Responsibilities:
Perform site management activities to support the client's Oncology site success and maintain a continuous state of inspection readiness
Act as the primary contact and facilitate efficient communications between the client's clinical trial team and the sites
Perform remote and on-site monitoring/co-monitoring visits (Site Qualification Visits, Site Initiation Visits, Interim Monitoring Visits and Close-Out Visits) to ensure data integrity and subject safety in the client's trials
May perform oversight activities to assess monitoring quality and train/mentor less experienced CRAs
Promptly document monitoring activities and submit/approve visit reports
Manage site essential document collection and TMF reconciliation with site files
Support sites with local Institutional Review Board (IRB)/Ethics Committee (EC) submissions and confirm approvals
Regularly review site Key Risk Indicator (KRI) metrics, issues and action items to detect trends and ensure prompt resolution
Independently determine root causes and develop/implement site Corrective Action and Preventive Action (CAPA) plans
Deliver training to ensure sites comply with the protocol, Standard Operating Procedures (SOPs), Good Clinical Practices (GCPs) and regulations
Support sites and the client's regulatory inspections
Contribute to site identification; drive site feasibility and qualification progress; and support site activation activities
Lead site engagement initiatives and foster relationships with key Oncology sites and networks
Qualifications
Bachelor’s degree (scientific field preferred)
5+ years monitoring clinical trials independently conducting on-site and remote monitoring visits. Atleast 2 years monitoring solid tumor clinical trials.
1+ years early development trial experience
Solid tumor clinical trial experience is required
Experience utilizing Veeva systems is highly preferred
Demonstrated experience developing/maintaining site relationships and securing compliance
Expertise in GxPs and Oncology monitoring techniques (including Risk-Based Monitoring) and terminology
Experience collaborating with sites from initial engagement through close-out phases
Experience activating sites
Experience training site staff
Experience supporting sites and/or sponsors in regulatory inspections
Experience working within a Functional Services (or in-house) monitoring model is preferred
Willing to travel up to 75%
Employment with ICON is contingent upon having the legal right to work in the country where the role is based.
Rewards & Benefits
ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.
Benefits may include:
- Competitive base salary and performance related incentives
- Health and wellbeing programmes including medical, dental, and vision coverage where applicable
- Retirement and pension plans
- Life assurance and disability coverage
- Employee assistance programmes and wellbeing resources
- Learning and development opportunities through structured training and career pathways
Benefits may vary depending on role and location.
Visit our careers site to read more about the benefits ICON offers.
Inclusion and Accessibility
ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.
If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.
Salary Range
$110,520.00-$138,150.00
ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.
As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.
The Sr. Clinical Research Associate (Sr. CRA) will be responsible for performing investigative site management and monitoring activities throughout the clinical trial lifecycle. This Sr. CRA role will support the client's Oncology clinical trials to ensure data integrity, subject safety, and inspection readiness at the clinical investigative sites.
Responsibilities:
Perform site management activities to support the client's Oncology site success and maintain a continuous state of inspection readiness
Act as the primary contact and facilitate efficient communications between the client's clinical trial team and the sites
Perform remote and on-site monitoring/co-monitoring visits (Site Qualification Visits, Site Initiation Visits, Interim Monitoring Visits and Close-Out Visits) to ensure data integrity and subject safety in the client's trials
May perform oversight activities to assess monitoring quality and train/mentor less experienced CRAs
Promptly document monitoring activities and submit/approve visit reports
Manage site essential document collection and TMF reconciliation with site files
Support sites with local Institutional Review Board (IRB)/Ethics Committee (EC) submissions and confirm approvals
Regularly review site Key Risk Indicator (KRI) metrics, issues and action items to detect trends and ensure prompt resolution
Independently determine root causes and develop/implement site Corrective Action and Preventive Action (CAPA) plans
Deliver training to ensure sites comply with the protocol, Standard Operating Procedures (SOPs), Good Clinical Practices (GCPs) and regulations
Support sites and the client's regulatory inspections
Contribute to site identification; drive site feasibility and qualification progress; and support site activation activities
Lead site engagement initiatives and foster relationships with key Oncology sites and networks
Qualifications
Bachelor’s degree (scientific field preferred)
5+ years monitoring clinical trials independently conducting on-site and remote monitoring visits. Atleast 2 years monitoring solid tumor clinical trials.
1+ years early development trial experience
Solid tumor clinical trial experience is required
Experience utilizing Veeva systems is highly preferred
Demonstrated experience developing/maintaining site relationships and securing compliance
Expertise in GxPs and Oncology monitoring techniques (including Risk-Based Monitoring) and terminology
Experience collaborating with sites from initial engagement through close-out phases
Experience activating sites
Experience training site staff
Experience supporting sites and/or sponsors in regulatory inspections
Experience working within a Functional Services (or in-house) monitoring model is preferred
Willing to travel up to 75%
Employment with ICON is contingent upon having the legal right to work in the country where the role is based.
Rewards & Benefits
ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.
Benefits may include:
- Competitive base salary and performance related incentives
- Health and wellbeing programmes including medical, dental, and vision coverage where applicable
- Retirement and pension plans
- Life assurance and disability coverage
- Employee assistance programmes and wellbeing resources
- Learning and development opportunities through structured training and career pathways
Benefits may vary depending on role and location.
Visit our careers site to read more about the benefits ICON offers.
Inclusion and Accessibility
ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.
If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.
Salary Range
$110,520.00-$138,150.00See All 27 Clinical Research Jobs in District of Columbia
Find roles in District of Columbia that match your experience and apply in just a few clicks.
Find Clinical Research JobsClinical Research Jobs by City in District of Columbia
Where District of Columbia roles are concentrated, by current openings.
Clinical Research Job Market in District of Columbia
A snapshot from current District of Columbia openings, updated as new roles post.
Who's Hiring
- Children's National Hospital17
- Georgetown University3
- Johns Hopkins University3
- The Henry M. Jackson Foundation for the Advancement of Military Medicine2
- Parexel1
Top Industries Hiring
- Healthcare & Medical Services19
- Education5
- Science & Research2
- Biotechnology & Pharmaceuticals1
What District of Columbia Employers Look For
The qualifications that appear most often in clinical research jobs across District of Columbia.
- Bachelor's degree in life sciences, nursing, or a related health field required
- Prior experience coordinating or managing clinical trials under GCP guidelines
- Familiarity with FDA regulations and ICH guidelines governing clinical research
- CCRP or CCRC certification from ACRP or SoCRA strongly preferred
- Proficiency with electronic data capture systems such as REDCap or Medidata Rave
- Strong written communication skills for protocol development and IRB submissions
Clinical Research Jobs in District of Columbia: Frequently Asked Questions
How do you become a clinical research in District of Columbia?
Clinical research professionals in D.C. typically enter the field with a bachelor's degree in a life or health science, then pursue certification through the Association of Clinical Research Professionals or the Society of Clinical Research Associates. D.C. does not require a state-issued clinical research license, but CCRP or CCRC certification is treated as a near-standard requirement by federal agencies, academic medical centers, and NIH-affiliated institutions throughout the region.
Which companies hire clinical researchs in District of Columbia?
District of Columbia clinical research roles are posted by Children's National Hospital, Georgetown University, and Johns Hopkins University and others right now, based on current listings on Migrate Mate as of July 2026. The D.C. market is shaped heavily by federal health agencies and affiliated contractors, so a significant share of openings come through government-funded research programs and academic hospital systems.
Which District of Columbia cities have the most clinical research jobs?
Washington account for the largest concentration of clinical research openings in District of Columbia. Washington, D.C. anchors the market through its dense cluster of federal health agencies and academic medical centers, while Bethesda and Silver Spring draw heavily from NIH campuses and the life sciences corridor along the I-270 corridor in nearby Maryland.
Are there remote clinical research jobs in District of Columbia?
Yes, but they're selective. About 22% of clinical research openings tied to District of Columbia are remote or hybrid as of July 2026, reflecting that much of the work requires on-site patient contact, lab access, or secure federal facilities. The roles most likely to be remote or hybrid are regulatory affairs coordination, data management, medical writing, and sponsor-side monitoring positions.
How can I get hired as a clinical research in District of Columbia with little or no experience?
The most realistic entry point is a research coordinator role at an academic medical center or NIH-affiliated hospital, where many institutions run structured onboarding programs for recent graduates. MedStar Health, Children's National Hospital, and George Washington University Hospital regularly post entry-level coordinator positions that accept candidates with a relevant degree and no prior trial experience. Completing a Good Clinical Practice certification before applying and gaining exposure through volunteer or internship work at a D.C.-area IRB or research office strengthens a new applicant's profile considerably.
Where can I find and apply to clinical research jobs in District of Columbia?
You can find and apply to clinical research jobs in District of Columbia on Migrate Mate, which lists current openings across the region. Search the available roles, identify the ones that match your background and experience level, and apply directly to the positions that fit.
See All 27 Clinical Research Jobs in District of Columbia
Find roles in District of Columbia that match your experience and apply in just a few clicks.
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