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Sarah Jenkins
Remote Clinical Research Assistant jobs in the United States
Job type
Min. salary, $/year
Level
The demand for clinical research assistant remote jobs continues to grow as healthcare organizations and research institutions across the USA expand their clinical trial operations. With 500+ open positions available, this is an excellent time for detail-oriented professionals to join a flexible, fully remote team supporting groundbreaking medical research from anywhere in the country.
Successful candidates typically bring strong organizational skills, attention to detail, and familiarity with clinical trial protocols, data entry systems, and regulatory compliance standards. Employers reviewing clinical research assistant vacancies often look for excellent communication abilities, basic knowledge of medical terminology, and comfort working with electronic data capture tools. Adaptability and a collaborative mindset are equally valued, since much of the coordination happens virtually across distributed research teams.
Remote work in this field usually involves coordinating with study sites, managing documentation, and supporting data collection without needing a physical office presence. As more sponsors and research organizations embrace decentralized trials, clinical research assistant positions are becoming increasingly common nationwide, reflecting a broader shift toward flexible, technology-driven healthcare research models throughout the USA.
If you are ready to advance your career in clinical research, now is the perfect time to explore current openings. Organizations are eager to hire a clinical research assistant who brings precision and passion to every project, and Global Work AI connects motivated professionals with these rewarding remote opportunities every day.
UBC
Oversee clinical project operations, ensuring compliance with ICH/GCP and local regulations. Manage clinical monitoring and site management, including scheduling visits and tracking adherence to protocols. Review monitoring reports, assist with training, and serve as a liaison for project issues.
remote, United StatesFull TimeSenior (5+ years)
Lightship
Independently monitor clinical trial sites for compliance with protocols, ICH-GCP, and regulatory requirements. Conduct Source Data Verification (SDV) and Source Data Review (SDR), identify data trends and discrepancies, and implement corrective actions.
remote, Durham, NC, United StatesFull TimeMiddle (2-4 years)
Magnus Medical
Manage clinical monitoring activities for trials, including site selection, initiation, monitoring, and close-out. Ensure adherence to protocols and regulatory guidelines, while providing operational leadership and mentoring junior staff.
remote, United States$140k – $165k/yrFull TimeSenior (5+ years)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)
Worldwide 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, CA, United States$80k – $159k/yrFull TimeMiddle (2-4 years)
Parexel
Manage site monitoring and close-out of clinical trials, ensuring compliance with GCP and client standards. Serve as the primary contact for investigator sites, addressing protocol-related issues and facilitating communication with the study team.
remote, AZ, United StatesFull TimeSenior (5+ years)
AtriCure
Manage assigned clinical investigative sites, assist with study protocol implementation, and conduct clinical monitoring. Coordinate site activities from start-up to closure, including protocol review, informed consent development, and site training.
remote, United States$85k – $105k/yrFull TimeMiddle (2-4 years)
Premier Research
Deliver quality monitoring reports per Clinical Monitoring Plan timelines. Ensure validity and completeness of clinical data at assigned sites according to ICH GCP/ISO14155 and protocol requirements. Conduct remote and on-site monitoring focused on data integrity and subject safety.
remote, United StatesFull TimeSenior (5+ 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)
Mass General Brigham
Design and execute experiments in transplantation immunology, collect and analyze data, and maintain laboratory notebooks. Collaborate with principal investigators to draft manuscripts and present findings at conferences.
remote, United States$41k – $58k/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 assess site performance throughout the study lifecycle.
remote, CA, United States$97k – $193k/yrFull TimeSenior (5+ years)Worldwide Clinical Trials
Manage clinical research activities at investigative sites, ensuring compliance with protocol and regulatory standards. Conduct monitoring visits including Pre-Site Selection, Study Initiation, Interim Monitoring, and Closeout Visits.
remote, United States$97k – $193k/yrFull TimeSenior (5+ 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)Parexel
Manage site monitoring and close-out of clinical trials, ensuring compliance with GCP and regulatory standards. Serve as the primary contact for investigator sites, facilitating communication and resolving protocol-related issues.
remote, AZ, United StatesFull TimeSenior (5+ years)
Rho Inc
Collect, track, and review investigational site records and regulatory documents. Manage data in the clinical trials management system (CTMS) and assist with query resolution. Perform on-site and remote monitoring activities, ensuring compliance with protocols and regulations.
remote, United States$55k – $65k/yrFull 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)
CareDx, Inc.
Conduct site visits to ensure protocol adherence and data accuracy. Collaborate with study teams to drive study success and ensure compliance with regulations. Identify data collection issues in EDC systems and maintain study documentation.
remote, United States$100k – $130k/yrFull TimeSenior (5+ years)
National University
Support research project start-up activities, including establishing workflows, creating timelines, and drafting IRB applications. Conduct mixed-methods data collection and analysis, and draft research deliverables such as reports and publications.
remote, United StatesPart TimeJunior (<2 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)
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)
Avania
Oversee clinical trial activities at investigational sites, ensuring compliance with protocols and regulatory requirements. Conduct site initiation visits, monitor data accuracy, and prepare for audits. Write visit reports and assist in submissions to regulatory bodies.
remote, United States$90k – $110k/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 support study start-up and closeout activities.
remote, IA, United States$97k – $193k/yrFull TimeSenior (5+ years)
Novotech Global
Build relationships with site personnel to manage clinical trials efficiently. Collaborate with teams to prepare essential documents and support regulatory submissions. Monitor investigational sites according to ICH GCP guidelines and ensure participant rights are protected.
remote, Northeast, United States$70k – $140k/yrFull TimeMiddle (2-4 years)Novotech Global
Build relationships with site personnel to manage clinical trials efficiently. Collaborate with teams to prepare essential documents and support regulatory submissions. Monitor investigational sites according to ICH GCP guidelines, ensuring participant safety and data accuracy.
remote, South San Francisco, CA, United States$70k/yrFull TimeJunior (<2 years)Novotech Global
Build relationships with site personnel to manage clinical trials efficiently. Prepare site essential documents and support regulatory submissions. Monitor investigational sites according to ICH GCP and Clinical Monitoring Plan, ensuring participant rights and data accuracy.
remote, CA, United States$70k – $140k/yrFull TimeMiddle (2-4 years)Worldwide 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)Novotech Global
Build relationships with Principal Investigators and site personnel to manage clinical trials efficiently. Prepare site essential documents and support regulatory submissions.
remote, United States$70k – $140k/yrFull TimeMiddle (2-4 years)
Precision Medicine Group
Oversee study site management to ensure patient safety and data quality. Conduct on-site monitoring of clinical research studies, manage site start-up procedures, and assist with budget negotiations.
remote, United States$92k – $137k/yrFull TimeMiddle (2-4 years)
Precision for Medicine
Oversee study site management ensuring patient safety and data quality. Conduct site visits including pre-study, initiation, monitoring, and close-out. Manage site start-up procedures, including regulatory submissions and investigator contracts.
remote, United States$92k – $137k/yrFull TimeMiddle (2-4 years)
AstraZeneca
Manage the preparation, initiation, monitoring, and closure of clinical study sites. Ensure compliance with ICH-GCP guidelines and AstraZeneca procedures. Conduct site visits, monitor study conduct, and resolve study-related issues.
remote, DC, United States$112k – $168k/yrFull TimeMiddle (2-4 years)
CPC Clinical Research
Support project execution and management across various functional areas including Research Operations and Data Management. Perform quality control reviews, manage document submissions to the Trial Master File, and assist with User Acceptance Testing.
remote, Aurora, CO, United StatesFull TimeJunior (<2 years)CPC Clinical Research
Assist in project execution and management by preparing Master Plans, Resource Materials, and documentation for the Trial Master File. Support various functional areas including Research Operations and Data Management. Manage user access requests and assist with User Acceptance Testing (UAT).
remote, United States$39k – $44k/yrFull TimeJunior (<2 years)Emmes 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)10,000,000+ more jobs available!
