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Part Time Clinical Trial Rn Jobs in Virginia (NOW HIRING)

Covista

Part Time Clinical Nursing Faculty

Roanoke, VA

$38.50 - $52.50/hr

... BSN, RN to MSN, a Master of Science in Nursing (MSN) with six Specialty Tracks, and a Doctor of ... Chamberlain College of Nursing seeks Part-Time Clinical Nursing Faculty interested in teaching with ...

Covista

Part Time Clinical Nursing Faculty

Roanoke, VA · On-site

$38.50 - $52.50/hr

... BSN, RN to MSN, a Master of Science in Nursing (MSN) with six Specialty Tracks, and a Doctor of ... Chamberlain College of Nursing seeks Part-Time Clinical Nursing Faculty interested in teaching with ...

Covista

Part Time Clinical Nursing Instructor

Arlington, VA · On-site

$45.25 - $61.50/hr

... BSN, RN to MSN, a Master of Science in Nursing (MSN) with six Specialty Tracks, and a Doctor of ... Chamberlain College of Nursing seeks Part-Time Clinical Instructors interested in teaching students ...

Covista

Part Time Clinical Nursing Instructor

Arlington, VA

$45.25 - $61.50/hr

... BSN, RN to MSN, a Master of Science in Nursing (MSN) with six Specialty Tracks, and a Doctor of ... Chamberlain College of Nursing seeks Part-Time Clinical Instructors interested in teaching students ...

Covista

Capstone Part-Time Clinical Nursing Faculty

Norfolk, VA · On-site

$38 - $51.75/hr

... BSN, RN to MSN, a Master of Science in Nursing (MSN) with six Specialty Tracks, and a Doctor of ... Chamberlain College of Nursing seeks Part-Time Clinical Nursing Faculty interested in teaching with ...

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Part Time Clinical Trial Rn information

What is the difference between Part Time Clinical Trial Rn vs Part Time Research Nurse?

AspectPart Time Clinical Trial RnPart Time Research Nurse
CredentialsRegistered Nurse (RN) license, clinical trial certificationsRegistered Nurse (RN) license, research-specific training
Work EnvironmentClinical trial sites, hospitals, research facilitiesResearch settings, hospitals, clinics
Employer & IndustryPharmaceutical companies, CROs, research institutionsAcademic institutions, hospitals, research organizations
Job FocusManaging clinical trial procedures, patient care in trialsSupporting research studies, data collection, patient monitoring

Both roles require RN licensure and involve working in research environments. The main difference lies in their focus: Part Time Clinical Trial Rns primarily manage clinical trial procedures and patient care within trials, while Part Time Research Nurses support research activities, data collection, and study coordination. Understanding these distinctions helps candidates choose the role that best fits their skills and career goals.

What is a Part Time Clinical Trial RN?

A Part Time Clinical Trial RN (Registered Nurse) is a nurse who works on a part-time basis to support clinical research studies. They are responsible for administering study medications, monitoring patient health, collecting data, and ensuring that trials adhere to regulatory and ethical standards. This role often involves working closely with physicians, research coordinators, and patients to facilitate the safe and effective conduct of clinical trials. Part Time Clinical Trial RNs typically have flexible schedules and may work in hospitals, research centers, or outpatient clinics.

How does a part-time Clinical Trial RN typically balance patient care with research documentation responsibilities?

As a part-time Clinical Trial RN, you will often need to efficiently manage your time between direct patient care—such as administering investigational medications and monitoring for side effects—and completing detailed research documentation required for regulatory compliance. Many RNs find that staying organized and proactively communicating with the research team helps manage these dual responsibilities. You'll likely work closely with principal investigators, coordinators, and other healthcare professionals to ensure both patient safety and accurate data collection, often attending regular team meetings to discuss trial progress and any patient concerns.

What are the key skills and qualifications needed to thrive as a Part Time Clinical Trial RN, and why are they important?

To thrive as a Part Time Clinical Trial RN, you need a solid background in nursing practice, clinical research protocols, and a valid RN license, often with experience in clinical trials or research settings. Familiarity with electronic data capture (EDC) systems, Good Clinical Practice (GCP) guidelines, and regulatory documentation is typically required. Attention to detail, strong organizational skills, and the ability to communicate effectively with both patients and research teams are standout soft skills. These competencies ensure accurate data collection, patient safety, and compliance with study protocols, which are critical for successful clinical research outcomes.
What are the most commonly searched types of Clinical Trial Rn jobs in Virginia? The most popular types of Clinical Trial Rn jobs in Virginia are:
What cities in Virginia are hiring for Part Time Clinical Trial Rn jobs? Cities in Virginia with the most Part Time Clinical Trial Rn job openings:
Part Time 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

This job post has expired today. Applications are no longer accepted.

George Mason University rating

8.3

Company rating: 8.3 out of 10

Based on 19 frontline employees who took The Breakroom Quiz

108th of 555 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/

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