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Clinical Trial Rn Jobs in Washington (NOW HIRING)

Axle

Clinical Research Coordinator

Bethesda, MD · On-site

$26 - $34.50/hr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Nursing Software * Experience with clinical trial management systems and research database Skills * Experience with technology transfer agreements, clinical trial agreements, cooperative research and ...

Georgetown University

Clinical Research Coordinator

Washington, DC · On-site

$27.50 - $36.75/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

The CRC2 is responsible for learning the schedule of assessments for each trial, and for ... Nursing * Occupational health * Emergency Medical Technician Work Mode Designation This position ...

Icon plc

Clinical Research Nurse II/Sonographer

Washington, DC

$68K - $85K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

... (RN) in the applicable jurisdiction. * Minimum of 2-3 years of clinical nursing experience, preferably in a research or academic healthcare setting, with demonstrated knowledge of clinical trial ...

Guidehouse

Clinical Program Manager

Bethesda, MD · On-site

$85K - $141K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Clinical Trial Operations Travel Required: None Clearance Required: Ability to Obtain Public Trust ... Master's degree in health and medical administrative services, nursing, or a related field.

IQVIA

Research Coordinator

Fairfax, VA · On-site

Current Texas or Virginia Registered Nursing License for RNs * Bachelor's degree required for non-RNs * Oncology clinical trial experience preferred * Research Coordination experience preferred Why ...

IQVIA

Research Coordinator

Fairfax, VA

Current Texas or Virginia Registered Nursing License for RNs * Bachelor's degree required for non-RNs * Oncology clinical trial experience preferred * Research Coordination experience preferred Why ...

Guidehouse

Clinical Program Manager

Bethesda, MD

$85K - $141K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Clinical Trial Operations Travel Required: None Clearance Required: Ability to Obtain Public Trust ... Master's degree in health and medical administrative services, nursing, or a related field.

IQVIA

Infusion Nurse - Fairfax, VA - On-site

Fairfax, VA

  • Medical

  • Life

  • PTO

Oncology Clinical Trial Practices * Confirms informed consent is documented prior to performing any ... Current Registered Nursing License in the state the role is based in for RNs * OCN preferred. * IV ...

IQVIA

Infusion Nurse - Fairfax, VA - On-site

Fairfax, VA · On-site

  • Medical

  • Life

  • PTO

Oncology Clinical Trial Practices * Confirms informed consent is documented prior to performing any ... Current Registered Nursing License in the state the role is based in for RNs * OCN preferred. * IV ...

IQVIA

Infusion Nurse

Fairfax, VA · On-site

$37.75 - $50/hr

  • Medical

  • Life

  • PTO

Oncology Clinical Trial Practices * Confirms informed consent is documented prior to performing any ... Current Registered Nursing License in the state the role is based in for RNs * OCN preferred. * IV ...

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Showing results 21-40

All JobsClinical Trial Rn JobsClinical Trial Rn Jobs in Washington

Clinical Trial Rn information

See Washington salary details

$32

$70

$108

How much do clinical trial rn jobs pay per hour?

As of Aug 15, 2026, the average hourly pay for clinical trial rn in Washington is $70.81, according to ZipRecruiter salary data. Most workers in this role earn between $57.45 and $79.76 per hour, depending on experience, location, and employer.

How to get into clinical trial registered nurse roles?

To become a clinical trial registered nurse, candidates typically need a valid RN license, relevant clinical experience, and specialized knowledge of research protocols and regulations. Obtaining certifications such as Certified Clinical Research Professional (CCRP) can enhance qualifications. Experience in oncology, cardiology, or other specialized areas is often preferred, along with familiarity with Good Clinical Practice (GCP) guidelines and trial management tools.

What are the typical responsibilities of a Clinical Trial RN?

As a Clinical Trial RN, your daily tasks often involve screening and enrolling study participants, administering investigational treatments, monitoring patient responses, and accurately documenting all trial data. You will collaborate closely with physicians, research coordinators, and other healthcare professionals to ensure adherence to study protocols and patient safety guidelines. Additionally, you may educate patients and their families about trial procedures and follow up with them throughout the study. This role combines patient care with administrative and regulatory responsibilities, offering a dynamic and meaningful work environment.

What is a Clinical Trial RN?

A Clinical Trial RN (Registered Nurse) is a specialized nurse who plays a key role in clinical research studies. They assist in patient recruitment, administer treatments, monitor patient responses, and ensure adherence to study protocols. They also collect and document data, work closely with principal investigators, and ensure compliance with regulatory guidelines. Their role is essential in advancing medical research and improving patient care through clinical trials.

Can nurses work in clinical trials?

Yes, nurses, including registered nurses (RNs), often work in clinical trials by assisting with patient care, monitoring participants, and collecting data. They typically need relevant clinical trial training, knowledge of Good Clinical Practice (GCP), and sometimes certification to ensure compliance with regulatory standards.

What are the key skills and qualifications needed to thrive as a Clinical Trial RN?

To thrive as a Clinical Trial RN, you need a solid background in nursing practice, current RN licensure, and an understanding of clinical research protocols. Familiarity with clinical trial management systems, electronic data capture tools, and Good Clinical Practice (GCP) certification is often required. Strong attention to detail, superior organizational abilities, and effective communication skills make candidates excel in this role. These competencies are crucial to ensure patient safety, regulatory compliance, and the accurate collection and reporting of trial data.

What are popular job titles related to Clinical Trial Rn jobs in Washington?

For Clinical Trial Rn jobs in Washington, the most frequently searched job titles are:

What job categories do people searching Clinical Trial Rn jobs in Washington look for?

The top searched job categories for Clinical Trial Rn jobs in Washington are:

Clinical Trial Rn jobs near you
Infographic showing various Clinical Trial Rn job openings in Washington as of August 2026, with employment types broken down into 2% As Needed, 74% Full Time, 18% Part Time, and 6% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $147,276 per year, or $70.8 per hour.

Clinical Research Coordinator

Axle

Bethesda, MD • On-site

$26 - $34.50/hr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 25 days ago

Job description

(ID: 2026-2878)
Axle is a bioscience and information technology company that offers advancements in translational research, biomedical informatics, and data science applications to research centers and healthcare organizations nationally and abroad. With experts in biomedical science, software engineering, and program management, we focus on developing and applying research tools and techniques to empower decision-making and accelerate research discoveries. We work with some of the top research organizations and facilities in the country including multiple institutes at the National Institutes of Health (NIH).
Axle is seeking a Clinical Research Coordinator to join our vibrant team at the National Institutes of Health (NIH) supporting the National Cancer Institute (NCI) located in Bethesda, MD.
Benefits We Offer:
  • 100% Medical, Dental & Vision Coverage for Employees
  • Paid Time Off and Paid Holidays
  • 401K match up to 5%
  • Educational Benefits for Career Growth
  • Employee Referral Bonus
  • Flexible Spending Accounts:
    • Healthcare (FSA)
    • Parking Reimbursement Account (PRK)
    • Dependent Care Assistant Program (DCAP)
    • Transportation Reimbursement Account (TRN)

Position Overview
The Contractor shall provide personnel capable of supporting complex clinical research portfolios and ensuring efficient coordination among investigators, research teams, oversight offices, regulatory agencies, collaborating institutions, and other stakeholders involved in the conduct of clinical research. Requires a Master's degree, along with preferred certifications such as SOCRA, FAC-P/M, FAC-COR, PMP, or ACRP credentials. Experience with clinical trial management systems and research databases, technology transfer or clinical trial agreements, and supporting NIH, NCI, academic medical centers, or federally funded research programs is preferred.
Additional Qualifications
Certifications & Licenses
  • SOCRA Certification
  • FAC-P/M Certification
  • FAC-COR Certification
  • PMP Certification
  • Association of Clinical Research Professionals (ACRP)

Field of Study
  • Health and Medical Administrative Services
  • Nursing

Software
  • Experience with clinical trial management systems and research database

Skills
  • Experience with technology transfer agreements, clinical trial agreements, cooperative research and development agreements, or related research partnerships
  • Experience supporting NIH, NCI, academic medical centers, or federally funded research programs

Deliverables
  • Monthly Activity Report - Monthly
  • Portfolio Status Report - Monthly
  • Risk Management Report - Monthly
  • Financial Status Report - Monthly
  • Regulatory Tracking Report - Monthly
  • Strategic Planning Support Reports - Ad-Hoc
  • Annual Program Summary Report - Yearly
  • Final Contract Summary Report - Ad-Hoc

Statement of Work Details
  • Coordinate operational activities for clinical studies - 1
  • Assist with feasibility assessments for proposed clinical trials - 2
  • Support startup activities for new studies - 3
  • Coordinate participating sites for multi-center trials - 4
  • Monitor study progress and enrollment-related metrics - 5
  • Reviews, assesses and evaluates clinical trial design and feasibility
  • Provide comprehensive management and oversight of assigned clinical research portfolios
  • Develop and maintain project management plans for clinical research projects
  • Monitor project schedules, timelines, deliverables, dependencies, and milestones
  • Track portfolio performance metrics and report progress to leadership
  • Assist Branch Chiefs and Program Leadership in prioritization of research activities
  • Support portfolio planning and resource allocation efforts
  • Monitor project execution to ensure alignment with organizational objectives
  • Reviews, evaluates and analyzes clinical trial data and study information
  • Lead development and maintenance of project-specific work plans
  • Coordinate project initiation, planning, execution, monitoring, and closeout activities
  • Facilitate project meetings and maintain meeting documentation
  • Track action items and follow-up activities
  • Monitor project performance and identify potential barriers to success
  • Assist investigators and research teams in achieving project objectives
  • Reviews, evaluates and recommends logistical, procedural and operational approaches to clinical trial implementation
  • Develop risk mitigation and response plans
  • Monitor identified risks throughout the project lifecycle
  • Escalate significant issues to leadership as appropriate
  • Coordinate corrective actions and resolution activities
  • Identify operational, regulatory, financial, and programmatic risks
  • Assesses and supports meetings, clinical trial assessments and site visits
  • Monitor and coordinate activities associated with protocol development, protocol amendments, IRB submissions, regulatory submissions, continuing reviews, study activation activities, and clinical trial monitoring activities
  • Support preparation for audits, inspections, and monitoring visits
  • Coordinate activities among investigators, regulatory staff, data managers, and clinical teams
  • Monitor compliance-related milestones and deliverables
  • Facilitate timely submission of required regulatory documents
  • Formulates guiding principles and Standard Operating Procedures (SOPs), and prepares staff for clinical research
  • Facilitate communication among study stakeholders
  • Assist with development of project-specific budgets
  • Monitor expenditures and financial performance
  • Track project funding and resource utilization
  • Develop financial forecasts
  • Identify potential budgetary concerns and recommend corrective actions
  • Prepare financial status reports for leadership review
  • Serve as liaison between assigned research programs and the Office of the Clinical Director (OCD), NCI Technology Transfer Center, regulatory offices, collaborating institutions, industry partners, and other NIH and NCI organizations
  • Coordinate leadership briefings and status updates
  • Prepare communication materials and project summaries
  • Assist Government personnel with development of Statements of Work
  • Assist with technical evaluations and acquisition planning activities
  • Track contractor performance, deliverables, and invoice status
  • Monitor contract milestones and option periods
  • Support COR activities as requested
  • Support strategic planning initiatives
  • Analyze program performance and operational effectiveness
  • Develop recommendations for process improvements
  • Assist leadership with prioritization of future research initiatives
  • Support implementation of organizational best practices

Disclaimer: The above description is meant to illustrate the general nature of work and level of effort being performed by individuals assigned to this position or job description. This is not restricted as a complete list of all skills, responsibilities, duties, and/or assignments required. Individuals may be required to perform duties outside of their position, job description or responsibilities as needed.
The diversity of Axle's employees is a tremendous asset. We are firmly committed to providing equal opportunity in all aspects of employment and will not tolerate any illegal discrimination or harassment based on age, race, gender, religion, national origin, disability, marital status, covered veteran status, sexual orientation, status with respect to public assistance, and other characteristics protected under state, federal, or local law and to deter those who aid, abet, or induce discrimination or coerce others to discriminate.
Accessibility: If you need an accommodation as part of the employment process please contact: careers@axleinfo.com
This role has a market-competitive salary with an anticipated base compensation range listed below. Actual salaries will vary depending on a candidate's experience, qualifications, skills, and location.
Salary Range
$145,000-$155,000 USD

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