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Sarah Jenkins
Remote Clinical Research Nurse jobs in the United States
Job type
Min. salary, $/year
Level
Health systems and research organizations throughout the United States are expanding their search for clinical research nurse remote jobs, reflecting the rapid growth of decentralized and virtual studies. With 500+ open positions now available, this remote role offers qualified nurses a chance to support patient safety and data accuracy from anywhere in the country.
Employers looking to hire a clinical research nurse typically value strong patient assessment skills, attention to regulatory detail, and experience with informed consent, protocol adherence, and electronic data capture systems. Excellent communication and the ability to coordinate with physicians, sponsors, and patients remain essential, along with adaptability to evolving trial technologies.
Remote nursing roles like this one continue to reshape how clinical trials are managed across the USA, as more sponsors adopt telehealth visits, digital monitoring platforms, and virtual check-ins for study participants. This shift has fueled steady demand for clinical research nurse vacancies, particularly among organizations seeking flexible, tech-savvy professionals who can manage remote patient interactions without sacrificing quality or compliance.
If you're ready to advance your nursing career, explore current opportunities available through Global Work AI. Discover a role that matches your expertise and compassion, and take the next step toward making a meaningful impact on patient care nationwide.
DotLab
Conduct independent site monitoring visits and remote monitoring to ensure compliance with study protocols and regulatory standards. Identify and escalate protocol deviations, data discrepancies, and noncompliance issues.
remote, New York, NY, United States$48k – $108k/yrFull TimeJunior (<2 years)
Humaneva Group
Perform monitoring and site management for Phase I-IV clinical research projects, ensuring compliance with regulatory and protocol standards. Serve as the primary liaison for project site personnel, conducting site evaluations, initiation, and close-out assessments.
remote, United StatesFull TimeSenior (5+ years)
Arbor Research Collaborative for Health
Lead the development of clinical content for training tools and provide technical assistance to health centers on SMBP workflow and quality improvement. Collaborate with evaluation teams to integrate findings into assistance activities and review reports before submission.
remote, DC, United States$54k – $88k/yrPart TimeLead / Manager
Memorial Sloan Kettering Cancer Center
Conduct innovative translational and clinical research, collaborate with scientists, and contribute to the understanding of cancer. Provide personalized care to patients and assist in training the next generation of scientists and clinicians.
remote, New York, NY, United StatesPart TimeJunior (<2 years)
Premier Research
Deliver quality monitoring reports for sponsor approval, ensuring compliance with Clinical Monitoring Plan timelines. Validate clinical data at assigned sites according to ICH GCP/ISO14155 and protocol requirements.
remote, United StatesFull TimeJunior (<2 years)
BeiGene
Conduct site visits to monitor compliance with protocols and regulations, ensuring data quality and patient safety. Build relationships with site personnel, provide training, and track site performance metrics.
remote, United States$92k – $122k/yrFull TimeMiddle (2-4 years)
Worldwide Clinical Trials
Manage clinical research activities at investigative sites, ensuring compliance with protocols and regulatory standards. Conduct monitoring visits, train site personnel, and assess site performance throughout the study lifecycle.
remote, CA, United States$97k – $193k/yrFull TimeSenior (5+ years)
Inova
Assist in preparing and submitting regulatory documents to sponsors and IRB. Conduct and document study visits and protocol-specific testing. Complete case report forms accurately according to the protocol. Perform study procedures relevant to training and certification.
remote, United StatesFull TimeEntry with Degree
ICON plc
Lead and coordinate project activities, ensuring timely and budget-compliant delivery. Develop and manage detailed project plans, including timelines and resource allocation. Monitor project progress, identify risks, and implement strategies to address challenges.
remote, Blue Bell, PA, United StatesFull TimeJunior (<2 years)
Professional Case Management
Provide virtual lifestyle counseling visits to improve nutrition and dietary quality for clinical trial subjects. Set appointments and complete visits within required timeframes.
remote, NM, United States$85k/yrPart TimeJunior (<2 years)Worldwide Clinical Trials
Manage clinical research activities at investigative sites, ensuring compliance with regulatory standards and protocol adherence. Conduct monitoring visits, train site personnel, and support study start-up and closeout activities.
remote, United States$97k – $193k/yrFull TimeSenior (5+ years)
Emmes Group
Assist with operational activities supporting site management and monitoring of clinical studies. Collect, review, maintain, and track essential documents, ensuring compliance with regulatory requirements. Update the Clinical Trial Management System and assist with trial progress tracking.
remote, United StatesFull TimeEntry with Degree
Linical
Conduct feasibility assessments, site initiation, monitoring, and close-out of clinical trial sites. Ensure compliance with Good Clinical Practices (GCPs) and regulatory requirements, verify data integrity, and manage site communications.
remote, United States$95k – $120k/yrFull TimeMiddle (2-4 years)Professional Case Management
Conduct mobile visits for study participants, performing physical assessments, blood specimen collection, and processing. Collaborate with Clinical Project Managers and site personnel to ensure accurate documentation and completion of Clinical Outcome Assessments.
remote, NJ, United States$121k/yrPart TimeJunior (<2 years)Lifelancer
Manage site relationships and perform on-site and remote monitoring for Phase I-IV clinical trials. Ensure compliance with ICH/GCP, local regulations, and SOPs. Conduct site initiation visits, deliver training, and monitor data integrity and patient safety.
remote, CA, United States$109k – $202k/yrFull TimeSenior (5+ years)
Baptist Health South Florida
Direct the development and coordination of the clinical research program. Enhance translation of evidence to practice for quality patient care. Provide guidance for nursing and inter-professional research studies.
remote, FL, United States$101k – $134k/yrFull TimeLead / ManagerUBC
Lead project teams to ensure project milestones are met, overseeing all aspects from study start-up to close-out. Develop and design protocols, regulatory documents, and project plans. Supervise project management staff, facilitate investigator meetings, and ensure compliance with operational plans.
remote, United StatesFull TimeSenior (5+ years)
Lycia Therapeutics
Monitor clinical trial sites to ensure compliance with protocols and regulations. Assist with investigator recruitment, site selection, and study startup tasks. Conduct remote monitoring activities and support traveling CRAs.
remote, South San Francisco, CA, United States$125k – $150k/yrFull TimeJunior (<2 years)
Prolific Academic Ltd
Complete expert registration and medical-credential verification through Prolific’s onboarding process. Participate in assessments to establish suitability for projects.
remote, United States$262k/yrPart TimeJunior (<2 years)
Care Access
Promote clinical research awareness and education in diverse communities. Support Future of Medicine events, deliver participant education, and assist with informed consent. Collaborate with local teams to standardize educational materials and capture lessons learned from events.
remote, United States$60k – $90k/yrFull TimeMiddle (2-4 years)
RTI International
Lead multi-site clinical research projects, including randomized clinical trials. Oversee study design, protocol development, implementation, quality control, data analysis, and presentation of results.
remote, United States$197k – $241k/yrFull TimeSenior (5+ years)UBC
Oversee all aspects of clinical project conduct from start-up through close-out. Manage project scope, budget, revenue, and invoicing. Develop project plans and ensure compliance with UBC and client SOPs. Serve as primary contact with sponsors and coordinate project meetings with stakeholders.
remote, United StatesFull TimeLead / Manager
Science 37
Provide mobile clinical nurse services to study participants at home, ensuring compliance with regulations and Good Clinical Practice. Collaborate with other nurses and study team members to develop solutions and support clinical trial implementation.
remote, United States$101k – $111k/yrPart TimeJunior (<2 years)RTI International
Support participant-centered health data collection in mobile clinic settings, coordinate training sessions, track data collection activities, conduct quality reviews, develop project materials, test questionnaires, and support IRB protocols.
remote, United States$74k – $91k/yrFull TimeMiddle (2-4 years)Prolific Academic Ltd
Complete expert registration and medical-credential verification through Prolific’s onboarding process. Participate in assessments to establish suitability for projects.
remote, United States$262k/yrPart TimeJunior (<2 years)
American Heart Association
Lead the implementation of industry-sponsored clinical research and quality improvement initiatives. Collaborate with industry partners to develop innovative research programs. Manage project plans, timelines, budgets, and communication strategies.
remote, Dallas, TX, United States$120k – $140k/yrFull TimeDirector
Perelman School of Medicine at the University of Pennsylvania
Coordinate clinical research activities for the Philadelphia Wellness Initiative, overseeing day-to-day operations of the interventional sub-study. Lead recruitment of primary care patients, manage regulatory documentation, and ensure protocol adherence and participant safety.
remote, PA, United States$53k – $58k/yrFull TimeJunior (<2 years)
Next Move Healthcare
Conduct research and evaluations of medical supplies and equipment across various healthcare settings. Perform functional equivalency assessments and compare product specifications to determine clinical suitability.
remote, United States$121k/yrFull TimeMiddle (2-4 years)Professional Case Management
Conduct mobile visits for study participants, performing blood specimen collection and processing. Collaborate with Clinical Project Managers and site personnel to ensure accurate documentation and timely completion of visits.
remote, United States$111k/yrPart TimeJunior (<2 years)Worldwide Clinical Trials
Manage clinical research activities at investigative sites, ensuring compliance with protocols and regulatory standards. Conduct monitoring visits, train site personnel, and support study start-up and closeout activities.
remote, IA, United States$97k – $193k/yrFull TimeSenior (5+ years)
Akero Therapeutics
Serve as Global Study Lead for a Phase 3 clinical study, overseeing operational planning, execution, and delivery. Lead study start-up, enrollment, site management, and ongoing conduct through CRO partners. Manage CROs and external vendors, ensuring alignment on priorities and deliverables.
remote, United States$153k – $267k/yrFull TimeLead / ManagerWorldwide Clinical Trials
Manage clinical research activities at investigative sites, ensuring compliance with protocol and regulatory standards. Conduct monitoring visits, train site personnel, and support study start-up and closeout activities.
remote, IA, United States$97k – $193k/yrFull TimeSenior (5+ years)Worldwide Clinical Trials
Manage research activities at investigative sites, supporting the full study lifecycle from site identification to close-out. Conduct Study Initiation Visits (SIVs), train sites on data collection, and ensure compliance with regulatory requirements.
remote, DC, United States$97k – $193k/yrFull TimeSenior (5+ years)
University of New Mexico
Lead the Rural Health Transformation Program by assessing and evaluating models of care to enhance access and quality of healthcare for rural populations. Develop and implement care models and service options based on needs assessments.
remote, NM, United States$7k – $10k/yrFull TimeDirector
Sequel Med Tech
Design and support real-world evidence studies, develop study protocols, and lead clinical research execution. Collaborate with internal teams and external partners to generate evidence for regulatory submissions and market access.
remote, Manchester, NH, United States$170k – $220k/yrFull TimeDirectorEmmes Group
Monitor clinical study sites remotely and on-site, ensuring compliance with protocols, SOPs, ICH GCP, and regulations. Conduct site visits including ICF review, source data verification, and investigator site file review.
remote, United StatesFull TimeSenior (5+ years)
Mass General Brigham
Coordinate and monitor multicenter oncology clinical trials, ensuring compliance with protocols and regulatory requirements. Maintain regulatory files, track trial progress, and facilitate communication with participating sites.
remote, United States$49k – $79k/yrFull TimeMiddle (2-4 years)
Syneos Health
Conduct site qualification, initiation, monitoring, management, and close-out visits, ensuring compliance with regulatory standards. Evaluate site performance, communicate issues, and develop action plans. Verify informed consent processes, assess patient safety, and ensure data integrity.
remote, United StatesFull TimeJunior (<2 years)
WEP Clinical
Provide nursing care to clinical trial participants in their homes, perform study-related procedures such as vital signs and specimen collection, administer investigational medications, conduct patient assessments, document visit activities, and educate patients on study procedures.
remote, OK, United States$101k – $111k/yrPart TimeJunior (<2 years)WEP Clinical
Provide nursing care to clinical trial participants in their homes, perform study-related procedures such as vital signs and specimen collection, administer investigational medications, conduct patient assessments, document visit activities, and educate patients on study procedures.
remote, TN, United States$101k – $111k/yrPart TimeJunior (<2 years)10,000,000+ more jobs available!
