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Remote Clinical Research Coordinator jobs in the United States
Job type
Min. salary, $/year
Level
The demand for a skilled clinical research coordinator continues to grow as healthcare organizations expand their trial capacity across the country. We currently have 500+ remote openings available for professionals ready to support clinical studies from anywhere in the USA. This is an excellent opportunity for candidates seeking flexible, meaningful work in the clinical research field.
Successful candidates typically bring strong organizational skills, attention to detail, and a solid understanding of regulatory compliance, including GCP and IRB protocols. Familiarity with electronic data capture systems, patient recruitment strategies, and clear communication with investigators and sponsors is essential. Employers looking to hire a clinical research coordinator often prioritize candidates who can manage multiple studies simultaneously while maintaining accuracy and adherence to timelines.
Remote work has become increasingly common for clinical research coordinator positions, as many administrative and monitoring tasks can be performed digitally without sacrificing quality or compliance. Across the USA, healthcare and pharmaceutical companies are expanding their remote teams to access a wider talent pool and reduce overhead costs. This shift has created steady demand for clinical research coordinator jobs in the USA, particularly among professionals comfortable with virtual collaboration tools and digital trial management systems.
If you are exploring clinical research coordinator vacancies and want a flexible, rewarding career path, now is the time to act. Browse current clinical research coordinator positions on Global Work AI and find the opportunity that matches your skills and career goals. Take the next step toward a fulfilling remote role in clinical research today.
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)
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)
UVA Health
Lead the clinical research budgeting and billing program, ensuring compliance and efficiency. Oversee coverage analyses, develop and negotiate clinical trial budgets, and manage sponsor invoicing processes.
remote, United StatesFull TimeLead / Manager
ERMI
Identify, screen, consent, and enroll research participants per study protocols. Coordinate participant visits and follow-up appointments, perform range-of-motion measurements, and maintain study data in electronic data capture systems.
remote, FL, United StatesPart 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)
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
Jobgether
Support planning, execution, oversight, and delivery of clinical trials from start-up through closeout. Manage assigned studies, develop and track study timelines, and coordinate activities across teams, CROs, and clinical sites.
remote, United States$110k – $120k/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)
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)
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)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
Kumquat Biosciences Inc
Lead the planning, monitoring, and execution of oncology clinical trials. Ensure compliance with regulatory guidelines and company protocols. Mentor junior CRAs and site personnel, manage trial documentation, and assist in regulatory submissions.
remote, San Diego, CA, United StatesFull TimeSenior (5+ years)
Jazz Pharmaceuticals
Manage clinical monitoring activities for investigator sites in Jazz-sponsored trials. Perform on-site and remote monitoring visits, provide mentorship to CRAs, and ensure compliance with protocols and regulations.
remote, United States$122k – $182k/yrFull TimeLead / Manager
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)
Fortrea
Conduct all aspects of study site monitoring, including routine monitoring, close-out of clinical sites, and maintenance of study files. Ensure compliance with informed consent procedures and protocol requirements.
remote, Northeast, United States$125k – $142k/yrFull TimeSenior (5+ 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)
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 protocols and regulatory standards. Conduct monitoring visits, train site personnel, and support study start-up and closeout activities.
remote, CT, 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, 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 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)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!
