Clinical Trials Nurse | PART-TIME
Portsmouth, VAPosted Apr 4, 2026
Behavioral Health Market Context
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Job Description
ccelerate the discovery and development of therapies with intelligent precision-ultimately improving patient outcomes globally.
Position Title Clinical Research Nurse (CRN)
Position Status Part-time (up to 20 hrs/wk).
Position Summary The Clinical Research Nurse (CRN) works collaboratively with the Clinical Research Coordinator (CRC), Principal Investigators and clinical site personnel to support clinical trial execution. This role combines nursing expertise with research responsibilities, including participant assessment, informed consent, protocol implementation, data quality oversight, and ensuring compliance with regulatory and DoD requirements. The CRN plays a key role in safeguarding participant safety, maintaining data integrity, and supporting operational excellence within military treatment facilities (MTFs) and other study sites.
Clinical Operations Reports to :
Clinical Operations Study Manager
Education Bachelor of Science in Nursing (BSN) preferred
Licensure Active RN license required for Virginia
Clinical Experience Minimum 2 years of clinical nursing experience required
Research Experience At least 1 year of clinical research experience strongly preferred. Regulatory and IRB experience preferred.
DOD Site Requirements Ability to obtain and maintain a security clearance per US government requirements.
Up to date immunizations.
Core Skills & Experience Strong foundation in clinical nursing practice, patient assessment, and clinical documentation.
Understanding of clinical research operations, GCP, and human subjects protections.
Proficiency with Microsoft Office, EDC systems, and remote collaboration tools.
Experience within DoD, VA, or other US government healthcare environments is highly desirable.
Working knowledge of the DoD Military Health System and clinical workflows within MTFs.
Experience with EHR systems such as MHS GENESIS (Cerner) preferred.
Job Responsibilities Conduct clinical assessments, vital signs, and study procedures within scope of nursing practice.
Administer investigational products (as permitted), observe participants, and document clinical findings per protocol.
Serve as a liaison among site clinicians, research teams, and military medical personnel.
Support protocol adherence, report deviations, and assist with site readiness for audits and monitoring visits.
Collaborate with CRCs on regulatory documentation, participant tracking, and study logistics.
Provide subject-matter expertise on clinical procedures, workflow optimization, and nursing considerations in protocol execution.
Schedule flexibility to support calls related to patients that may occur early in the morning or late in the evening as well as potentially on the weekends.
Ability to perform protocol procedures as needed (e.g. phlebotomy, ECGs, biological specimen collection).
Assist with regulatory submissions as needed.
Extent of Travel Up to 25%, including travel to military treatment facilities and partner clinical sites.
Position Title Clinical Research Nurse (CRN)
Position Status Part-time (up to 20 hrs/wk).
Position Summary The Clinical Research Nurse (CRN) works collaboratively with the Clinical Research Coordinator (CRC), Principal Investigators and clinical site personnel to support clinical trial execution. This role combines nursing expertise with research responsibilities, including participant assessment, informed consent, protocol implementation, data quality oversight, and ensuring compliance with regulatory and DoD requirements. The CRN plays a key role in safeguarding participant safety, maintaining data integrity, and supporting operational excellence within military treatment facilities (MTFs) and other study sites.
Clinical Operations Reports to :
Clinical Operations Study Manager
Education Bachelor of Science in Nursing (BSN) preferred
Licensure Active RN license required for Virginia
Clinical Experience Minimum 2 years of clinical nursing experience required
Research Experience At least 1 year of clinical research experience strongly preferred. Regulatory and IRB experience preferred.
DOD Site Requirements Ability to obtain and maintain a security clearance per US government requirements.
Up to date immunizations.
Core Skills & Experience Strong foundation in clinical nursing practice, patient assessment, and clinical documentation.
Understanding of clinical research operations, GCP, and human subjects protections.
Proficiency with Microsoft Office, EDC systems, and remote collaboration tools.
Experience within DoD, VA, or other US government healthcare environments is highly desirable.
Working knowledge of the DoD Military Health System and clinical workflows within MTFs.
Experience with EHR systems such as MHS GENESIS (Cerner) preferred.
Job Responsibilities Conduct clinical assessments, vital signs, and study procedures within scope of nursing practice.
Administer investigational products (as permitted), observe participants, and document clinical findings per protocol.
Serve as a liaison among site clinicians, research teams, and military medical personnel.
Support protocol adherence, report deviations, and assist with site readiness for audits and monitoring visits.
Collaborate with CRCs on regulatory documentation, participant tracking, and study logistics.
Provide subject-matter expertise on clinical procedures, workflow optimization, and nursing considerations in protocol execution.
Schedule flexibility to support calls related to patients that may occur early in the morning or late in the evening as well as potentially on the weekends.
Ability to perform protocol procedures as needed (e.g. phlebotomy, ECGs, biological specimen collection).
Assist with regulatory submissions as needed.
Extent of Travel Up to 25%, including travel to military treatment facilities and partner clinical sites.
Qualifications
- •Licensure Active RN license required for Virginia
- •Clinical Experience Minimum 2 years of clinical nursing experience required
- •DOD Site Requirements Ability to obtain and maintain a security clearance per US government requirements
- •Up to date immunizations
- •Core Skills & Experience Strong foundation in clinical nursing practice, patient assessment, and clinical documentation
- •Understanding of clinical research operations, GCP, and human subjects protections
- •Proficiency with Microsoft Office, EDC systems, and remote collaboration tools
- •Working knowledge of the DoD Military Health System and clinical workflows within MTFs
Benefits
Responsibilities
- •Position Status Part-time (up to 20 hrs/wk)
- •Position Summary The Clinical Research Nurse (CRN) works collaboratively with the Clinical Research Coordinator (CRC), Principal Investigators and clinical site personnel to support clinical trial execution
- •This role combines nursing expertise with research responsibilities, including participant assessment, informed consent, protocol implementation, data quality oversight, and ensuring compliance with regulatory and DoD requirements
- •The CRN plays a key role in safeguarding participant safety, maintaining data integrity, and supporting operational excellence within military treatment facilities (MTFs) and other study sites
- •Job Responsibilities Conduct clinical assessments, vital signs, and study procedures within scope of nursing practice
- •Administer investigational products (as permitted), observe participants, and document clinical findings per protocol
- •Serve as a liaison among site clinicians, research teams, and military medical personnel
- •Support protocol adherence, report deviations, and assist with site readiness for audits and monitoring visits
- •Collaborate with CRCs on regulatory documentation, participant tracking, and study logistics
- •Provide subject-matter expertise on clinical procedures, workflow optimization, and nursing considerations in protocol execution
- •Schedule flexibility to support calls related to patients that may occur early in the morning or late in the evening as well as potentially on the weekends
- •Ability to perform protocol procedures as needed (e.g. phlebotomy, ECGs, biological specimen collection)
- •Assist with regulatory submissions as needed
- •Extent of Travel Up to 25%, including travel to military treatment facilities and partner clinical sites
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