1:00 PM - 2:00 PM
Senior Product Manager Interview
Sarah Jenkins
Remote Clinical Trial Assistant jobs in the United States
Job type
Min. salary, $/year
Level
Demand for clinical trial assistant remote jobs is rising across the USA as pharmaceutical and biotech companies expand decentralized studies. With 500+ open positions available, this is an ideal time for detail-oriented professionals to join this growing role supporting research teams nationwide and managing essential documentation for ongoing studies.
Successful candidates for clinical trial assistant vacancies typically show strong organizational skills, attention to detail, and familiarity with regulatory compliance guidelines. Employers value proficiency in managing regulatory documents, maintaining research files, and communicating with investigators and sponsors. Experience with trial management systems and electronic data capture tools, along with strong communication skills, is highly valued.
Remote work for this role in the USA often means virtual collaboration with research associates, data managers, and site coordinators across time zones. As sponsors increasingly adopt remote work models, hiring outlook remains strong nationwide, with many companies ready to hire a clinical trial assistant who can work independently using digital platforms.
If you're ready to advance your career in clinical research, explore current opportunities available through Global Work AI. Our platform connects skilled professionals with companies offering remote roles across the USA, helping you find a rewarding position in this growing field.
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)Washington University in St. Louis
Supervise and train research coordinators, ensuring compliance with clinical trial protocols. Oversee daily research activities, monitor data accuracy, and facilitate study accrual. Collaborate with administrative and medical directors to plan staffing and education for Functional Research Groups.
remote, United States$75k/yrFull TimeJunior (<2 years)
Worldwide Clinical Trials
Coordinate and track system access for project team members, maintain project portals, perform quality checks on documents, support preparation and distribution of clinical trial documentation, manage project documentation for the Trial Master File, track key project information, prepare meeting…
remote, United States$17k – $34k/yrFull TimeJunior (<2 years)
Generate Biomedicines
Support execution of Phase 3 clinical trials, including site activation, study conduct, and closeout activities. Manage Trial Master File (TMF) setup and maintenance, ensuring inspection-ready documentation. Collaborate with CROs on monitoring visit reports and protocol deviations.
remote, United States$79k – $103k/yrFull TimeJunior (<2 years)Worldwide Clinical Trials
Coordinate and track system access for project team members, maintain project portals, perform quality checks on documents, support preparation and distribution of clinical trial documentation, manage project documentation for the Trial Master File, track key project information, prepare meeting…
remote, United States$17k – $34k/yrFull TimeJunior (<2 years)DotLab
Manage operational aspects of clinical trials from start-up to close-out. Develop and review study-related documents, ensure compliance with protocols and regulations, and monitor clinical sites.
remote, New York, NY, United States$72k – $144k/yrFull TimeSenior (5+ years)
Emmes Group
Lead operational activities for clinical studies, ensuring timelines and quality are met. Oversee monitoring teams and deliverables, including clinical monitoring plans and site visit reports.
remote, United StatesFull TimeLead / Manager
Jobgether
Lead and oversee clinical research operations across multiple studies, ensuring quality and regulatory compliance. Manage the full clinical trial lifecycle, including feasibility assessments, study start-up, execution, monitoring, and closeout activities.
remote, United StatesFull TimeLead / Manager
Moffitt Cancer Center
Manage the startup of new clinical trials, ensuring adherence to institutional policies and activation timelines. Lead the study activation process, track progress updates, and collaborate with stakeholders to operationalize trials.
remote, AL, United States$67k – $102k/yrFull TimeMiddle (2-4 years)
Syneos Health
Oversee site management, clinical monitoring, and ensure compliance with protocols and regulations. Manage site interactions, patient recruitment, and investigator payments. Identify risks to clinical trial deliverables and escalate issues to project management.
remote, United StatesFull TimeJunior (<2 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 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)
TransPerfect
Evaluate study feasibility with Principal Investigators, complete feasibility questionnaires, and prepare IRB applications. Oversee daily study conduct ensuring compliance with protocols and regulations, manage participant recruitment, and ensure accurate data entry.
remote, United StatesFull TimeLead / Manager
BioAge Labs
Coordinate clinical trial activities from start-up to close-out, ensuring operational milestones and timelines are met. Manage the Trial Master File (TMF) for quality and compliance, perform ongoing quality control, and resolve documentation gaps.
remote, United States$80k – $90k/yrFull TimeSenior (5+ years)
Summit Therapeutics
Oversee site selection, feasibility, activation, enrollment, monitoring, and closeout activities for global clinical trials. Provide strategic leadership and operational oversight, ensuring high-quality study execution and data monitoring strategies.
remote, CA, United States$98k – $116k/yrFull TimeSenior (5+ years)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)
Tyra Biosciences
Manage and oversee CROs, study vendors, and clinical trial sites. Support clinical operations from protocol concept to clinical study report, including study set-up, regulatory submissions, and training manuals.
remote, United States$148k – $163k/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)
Johnson & Johnson Innovative Medicine
Manage clinical trials locally, ensuring compliance with protocols and regulations. Oversee trial operations from start-up to closeout, including site assessments, recruitment planning, and data quality.
remote, United StatesFull TimeSenior (5+ years)
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)Jobgether
Coordinate and track system access for clinical project team members, maintain project portals, and perform quality checks on documentation. Support the preparation and organization of clinical trial documentation and Investigator Site Files (ISFs).
remote, United States$32k – $67k/yrFull TimeJunior (<2 years)
Kriya Therapeutics
Manage day-to-day operations of clinical trials, ensuring compliance with SOPs and ICH/GCP guidelines. Lead study start-up, conduct, and close-out activities, including budget preparation and vendor negotiations.
remote, United StatesFull TimeSenior (5+ years)
Perspective Therapeutics
Provide administrative support to Clinical Operations, manage study documentation, facilitate site outreach, coordinate meetings, and oversee the electronic Trial Master File (eTMF) system.
remote, United StatesFull TimeJunior (<2 years)
Liquidia
Coordinate with Clinical Operations team and external partners to manage clinical trials. Assist in project start-up, including budgets and contracts, and oversee clinical project-related documents.
remote, United StatesFull TimeSenior (5+ years)
Merck
Manage end-to-end clinical site payment activities including configuring payment templates, setting up vendor and site information, and processing invoices. Support invoice submission and approval, perform data entry, and maintain accurate payment-related information.
remote, United States$54k – $58k/yrFull TimeJunior (<2 years)
Penfield Search Partners
Manage and execute clinical trial activities in compliance with GCP and regulatory requirements. Oversee regional clinical trial activities, coordinate cross-functional team efforts, and ensure timely, high-quality deliverables.
remote, Fairfield, CT, United StatesFull TimeLead / Manager
ICON plc
Oversee clinical trial management workstreams, ensuring deliverables meet quality and timeline expectations. Collaborate with cross-functional teams to design and implement clinical trial protocols. Manage day-to-day operations of clinical trials, ensuring compliance with regulatory standards.
remote, Blue Bell, PA, United StatesFull TimeLead / Manager
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)BeiGene
Support the Regional Clinical Study Manager in executing clinical studies, ensuring quality standards are met. Assist Clinical Research Associates with study delivery tasks, including document management and participant enrollment.
remote, United States$84k – $114k/yrFull TimeSenior (5+ years)
Advocate Health
Provide administrative support for research activities, ensuring timely proposal submissions and tracking approvals. Manage compliance with IRB, IACUC, and COI, and assist in the grants/contracts lifecycle.
remote, United States$62k – $93k/yrFull TimeJunior (<2 years)
Shoulder Innovations
Provide administrative support for clinical trial operations, manage documentation processes to meet regulatory requirements, assist in preparing and submitting IRB documents, monitor adherence to study protocols, track study data, and coordinate communications with study sites.
remote, Grand Rapids, MI, United StatesFull TimeJunior (<2 years)
Thermo Fisher Scientific
Manage clinical operational and quality aspects of studies, ensuring compliance with ICH GCP. Develop clinical tools and contribute to clinical documentation. Collaborate with the clinical team to meet project deliverables and maintain timelines.
remote, Wilmington, NC, United StatesFull TimeLead / Manager
Cardiovascular Associates of America
Manage financial activities for clinical trials, including budget development, negotiation, and financial setup in REALTIME CTMS. Perform monthly billing, quality control of invoices, and payment reconciliation.
remote, Celebration, FL, United StatesFull TimeSenior (5+ years)
Cogstate
Coordinate operational activities for clinical trials and Rater Services programs. Serve as a contact point for stakeholders, maintain study documentation, and support study start-up and close-out activities.
remote, United States$58k – $65k/yrFull TimeJunior (<2 years)Syneos Health
Lead and manage Clinical Trial Managers, ensuring quality in monitoring and site management activities. Act as the primary contact for monitoring strategy, oversee project financial performance, and analyze compliance metrics.
remote, United StatesFull TimeDirectorCogstate
Manage and execute tasks in line with company SOPs and regulatory standards, including accurate record keeping and real-time updates. Serve as the primary contact for sites and raters, ensuring timely delivery of project tasks.
remote, United States$65k – $75k/yrFull TimeLead / Manager
Iovance Biotherapeutics
Manage the operational execution of clinical studies from initial synopsis to final deliverables, including budget development and resource management. Oversee cross-functional teams to ensure compliance with timelines and quality standards.
remote, United States$145k – $165k/yrFull TimeLead / ManagerKriya Therapeutics
Coordinate clinical trial activities across study phases, ensuring compliance with protocols. Prepare and review study documents, drive communication with CROs and clinical sites, and track study milestones using CTMS.
remote, NC, United StatesFull TimeSenior (5+ years)
Yale New Haven Health
Analyze and resolve complex clinical trial patient accounts, ensuring accurate billing to insurance or clinical trial coordinators. Develop and implement billing procedures, produce computerized reports, and collaborate with various departments to meet financial and compliance objectives.
remote, New Haven, CT, United StatesFull TimeMiddle (2-4 years)10,000,000+ more jobs available!
