ZipRecruiter

Log In

1

Clinical Trial Rn Jobs in Washington (NOW HIRING)

Oran Inc

Clinical SME I

Herndon, VA · Remote

... * RN * MPH * MS in Clinical Research * Related clinical/scientific discipline * Minimum 10 years of relevant clinical research or regulatory experience. * Deep understanding of: * Clinical trial ...

Oran, Inc.

Clinical SME I

Herndon, VA · On-site

... * RN * MPH * MS in Clinical Research * Related clinical/scientific discipline * Minimum 10 years of relevant clinical research or regulatory experience. * Deep understanding of: * Clinical trial ...

Oran Inc

Clinical SME I

Herndon, VA · Remote

... * RN * MPH * MS in Clinical Research * Related clinical/scientific discipline * Minimum 10 years of relevant clinical research or regulatory experience. * Deep understanding of: * Clinical trial ...

Apply Early

Patterns Hiring, Inc.

Clinical Nurse

Fairfax, VA · On-site

Current Virginia Registered Nursing License for RNs * Oncology experience preferred * Clinical trial experience preferred Essential Duties and Responsibilities: Essential and other important ...

Avery Healthcare Group Ltd.

Clinical Nurse

Fairfax, VA · On-site

Current Virginia Registered Nursing License for RN's * Oncology experience preferred * Clinical trial experience preferred Why Join Us? At NEXT Oncology (an Avacare Business), you'll be part of a ...

IQVIA, Inc.

Clinical Nurse

Fairfax, VA · On-site

Current Registered Nursing License for the state the role is based in for RN's * Oncology experience preferred * Clinical trial experience preferred Why Join Us? At NEXT Oncology (an Avacare Business ...

IQVIA

Clinical Nurse

Fairfax, VA

Current Registered Nursing License for the state the role is based in for RN's * Oncology experience preferred * Clinical trial experience preferred Why Join Us? At NEXT Oncology (an Avacare Business ...

IQVIA

Clinical Nurse

Fairfax, VA

Current Registered Nursing License for the state the role is based in for RN's * Oncology experience preferred * Clinical trial experience preferred Why Join Us? At NEXT Oncology (an Avacare Business ...

IQVIA

Research Coordinator

Arlington, 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 ...

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 ...

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

Arlington, 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 ...

next page

Showing results 1-20

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 Jul 2, 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 make $150,000 as a nurse?

A Clinical Trial RN can earn $150,000 by gaining specialized certifications, working in high-paying regions, and taking on overtime or leadership roles in clinical research. Building experience in complex trials and working for large pharmaceutical companies or research organizations can also increase earning potential.

What are some typical responsibilities of a Clinical Trial RN on a day-to-day basis?

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 job?

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.

How to make $300,000 as a nurse?

A Clinical Trial RN can increase earning potential by gaining specialized certifications, such as in clinical research or pharmacology, and working in high-paying settings like pharmaceutical companies or research organizations. Combining full-time clinical trial work with consulting or teaching roles can also boost income, but reaching $300,000 typically requires advanced experience, additional certifications, and possibly working overtime or in leadership positions.

What are the key skills and qualifications needed to thrive in the Clinical Trial Rn position, and why are they important?

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 do clinical trial nurses do?

Clinical trial nurses are responsible for coordinating and managing patient care during clinical research studies. They screen participants, administer treatments, monitor health status, collect data, and ensure compliance with study protocols and safety regulations. Their role requires strong clinical skills, attention to detail, and knowledge of research guidelines.

How to make 200,000 a year as a nurse?

A Clinical Trial RN can earn $200,000 annually by gaining specialized certifications, such as in clinical research coordination or management, and working in high-paying settings like pharmaceutical companies or research organizations. Increasing experience, taking on leadership roles, and working overtime or multiple jobs can also boost income, especially in regions with higher pay scales.
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
School of Nursing - Clinical Trial Coordinator

School of Nursing - Clinical Trial Coordinator

George Mason University

Fairfax, VA • On-site

Part-time

Posted 21 days ago

George Mason University rating

8.3

Company rating: 8.3 out of 10

Based on 19 frontline employees who took The Breakroom Quiz

97th of 544 rated colleges and universities

Job description

Department: College of Public Health
Classification: GMU Worker
Job Category: Part-Time / Hourly Wage
Job Type: Part-Time
Location: Fairfax, VA
Workplace Type: On Site Required
Sponsorship Eligibility: Not eligible for sponsorship
Salary: Salary commensurate with education and experience
Criminal Background Check: Yes
About the Department:
For more than 50 years, George Mason University's School of Nursing has prepared students for interdisciplinary roles as clinicians, educators, researchers, and administrators. Faculty contribute to the health of all populations through innovative and impactful education, research, practice, and service. The school enrolls a large and diverse student body across baccalaureate, master's, and doctoral programs offered in on-campus, hybrid, and online formats. Academic offerings include BSN programs (traditional, accelerated second degree, RN-to-BSN, and co-enrollment), MSN programs, a Doctor of Nursing Practice (DNP) program with concentrations in family practice, psychiatric mental health, adult-gerontology, and administration, and a PhD in Nursing program. BSN, MSN, and DNP degrees are accredited by the Commission on Collegiate Nursing Education (CCNE). The school is nationally recognized for its innovation in immersive technologies, simulation accreditation, and partnerships with healthcare providers serving culturally diverse populations in Northern Virginia, equipping graduates with the skills to deliver high-quality care where it is needed most. Further information about the school may be found at: https://nursing.gmu.edu .
About the Position:
The Clinical Trial Coordinator will support the operational, regulatory, and administrative management of clinical research studies conducted under the Clinical Research Operations and Management System (CROMS). This position plays a critical role in ensuring that clinical trials are conducted in compliance with federal regulations, institutional policies, and sponsor requirements. The Clinical Trial Coordinator will work closely with Principal Investigator (PI) and research staff to support the successful execution of grant-funded clinical research projects. This is a grant-funded position.
Responsibilities:
Clinical Trial Operations
  • Coordinate day-to-day operations of assigned clinical trials from study start-up through close-out;
  • Assist with participant recruitment, screening, enrollment, scheduling, and follow-up activities in accordance with approved protocols;
  • Maintain accurate and up-to-date study documentation, including source documents, case report forms, and study logs; and
  • Ensure protocol adherence and promptly identify, document, and report protocol deviations.

Regulatory and Compliance Support
  • Assist with preparation, submission, and maintenance of regulatory documents to Institutional Review Boards (IRBs), sponsors, and regulatory agencies;
  • Ensure compliance with federal regulations and institutional policies;
  • Support adverse event and serious adverse event reporting in coordination with the PI;
  • Maintain regulatory binders and CROMS documentation systems in an audit-ready state; and
  • Assist with REDCap survey design, implementation, data collection, and data management to support research protocols.

Data and Systems Management
  • Enter, review, and maintain study data in CROMS and other electronic data capture systems;
  • Perform data quality checks and resolve data queries in collaboration with investigators and sponsors; and
  • Assist with preparation for monitoring visits, audits, and inspections.

Communication and Collaboration
  • Serve as a liaison between investigators, sponsors, CROs, CROMS staff, and clinical sites;
  • Participate in study meetings, investigator meetings, and training sessions as required;
  • Communicate study progress, issues, and timelines to the research team and CROMS leadership; and
  • Provide translation support for research survey measures and conduct interviews with participants in English and either Spanish or Korean.

Administrative and Grant Support
  • Assist with tracking study milestones, timelines, and grant-related deliverables;
  • Support documentation for grant reporting, renewals, and progress updates as required; and
  • Maintain confidentiality of participant data and sensitive research information.

Required Qualifications:
  • Bachelor's degree in health sciences, public health, biological sciences, or a related field, or an equivalent combination of education and experience;
  • Demonstrated knowledge of clinical research processes and regulatory requirements;
  • Strong organizational skills with the ability to manage multiple studies and priorities;
  • Excellent written and verbal communication skills;
  • Proficiency with electronic research management systems and standard office software; and
  • Bilingual proficiency in English and either Korean or Spanish (written and verbal).

Preferred Qualifications:
  • Prior experience coordinating clinical trials or working in a clinical research environment;
  • Familiarity with CROMS, IRB submission systems, and electronic data capture platforms;
  • Training or certification in Good Clinical Practice or clinical research coordination; and
  • Experience working on grant-funded research projects.

Instructions to Applicants:
For full consideration, applicants must apply for Clinical Trial Coordinator (Req#10003756) at https://jobs.gmu.edu/. Complete and submit the online application to include three professional references with contact information, one of which is a most recent supervisor, and provide a cover letter and resume for review.
Posting Open Date: February 11, 2026
For Full Consideration, Apply by: February 25, 2026
Open Until Filled: Yes
Mason Ad Statement
George Mason University is a nationally ranked R1 research university committed to creating a more just, free, and prosperous world. With 40,000 enrolled students, George Mason is the largest and most diverse public research university in Virginia, offering degree programs at the master's, doctoral, and professional level, along with certificates and credentials.
George Mason fosters an All Together Different environment for students, faculty, and staff, driven by our core beliefs. We believe in inclusivity over exclusivity; we believe in advancing our mission by being willing to take risks, not avoiding them; and we believe our best work is possible when we apply our diversity of origin, identity, circumstance, and thought.
Equity Statement
George Mason University is an equal opportunity/affirmative action employer, committed to promoting inclusion and equity in its community. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability or veteran status, or any characteristic protected by law.
Campus Safety Information
Mason's Annual Security and Fire Safety Report is available at http://police.gmu.edu/annual-security-report/

What George Mason University employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom

Apply