2,317 Clinical Research jobs available for remote work from home. Apply for positions such as Biostatistical Analyst II (Remote Capable), Senior Clinical Research Associate - US - Oncology, Clinical Quality Compliance Manager, and more! Discover the best work-from-home or hybrid, full- and part-time jobs.
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Collaborate with clinical investigators to design research studies, develop analysis plans, and manage and interpret study data. Provide statistical consultations, prepare publication-quality graphics, and educate research staff on statistical methods.
Manage research activities at clinical sites, including site identification, start-up, and close-out activities. Conduct study initiation visits and ensure compliance with regulatory requirements and safety reporting.
Responsible for the execution, maintenance, and continuous improvement of the Quality Management System (QMS) and clinical trial quality oversight. This includes managing CAPA programs, conducting audits, and ensuring software development adheres to FDA and life sciences compliance standards.
Oversee clinical laboratory operations workstreams to ensure deliverables meet quality and timeline expectations. Act as the primary contact for clients regarding ICON Central Laboratories services and manage studies in accordance with Good Clinical Practice.
The role involves conducting risk assessments on clinical trial data to identify potential issues and recommend mitigation strategies. You will monitor data quality and integrity throughout the trial process and collaborate with cross-functional teams to implement risk management plans.
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Coordinate and perform remote clinical activities to collect and report patient data in compliance with study protocols and GCP. Manage virtual patient recruitment, enrollment, and informed consent processes while ensuring participant safety.
Lead the production of high-quality medical publications, abstracts, and posters from conception to completion. Act as the primary contact for clients and provide senior review, training, and mentorship to other writers.
The Regulatory Analyst I prepares and maintains regulatory documentation for clinical trials from start-up through closure. This includes managing submissions to boards and committees, ensuring compliance with FDA and NIH regulations, and maintaining the Trial Master File.
The Regulatory Analyst prepares and maintains regulatory documentation for clinical trials from start-up through closure. This includes managing submissions to boards and committees, ensuring compliance with FDA and NIH regulations, and updating Trial Master Files.
The role involves designing and executing clinical trial protocols, managing site selection, and overseeing data collection for Hematology and Hemostasis products. It also requires performing statistical analysis and authoring comprehensive final study reports for regulatory submission.
Drive growth through consultative sales of clinical research and laboratory services to pharmaceutical and biotech companies. Manage the full sales cycle from RFP strategy and proposal development to contract negotiation and client satisfaction.
Lead the end-to-end delivery of global clinical trials from start-up to close-out, ensuring compliance with ICH-GCP and company SOPs. Manage sponsor relationships, project budgets, and cross-functional teams to ensure studies are delivered on time and within budget.
The role involves acting as the primary contact for clinical trial sites and managing the site lifecycle from start-up to close-out. Responsibilities include conducting monitoring visits and ensuring compliance with study protocols and regulatory requirements.
Manage and negotiate contractual agreements for clinical research projects while ensuring alignment with regulatory requirements and company policies. Analyze contract terms to identify risks and provide guidance to project teams on compliance and contractual obligations.
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Develop and manage Investigator Grant Estimates and detailed study budgets for clinical trial proposals. Partner with stakeholders to create competitive costing strategies and drive process improvements in grants management.
Responsible for preparing and maintaining budgets for sponsored clinical trials and setting up payment milestones in the CTMS. Collaborates with contract analysts and regulatory teams to integrate budget information into clinical trial agreements and manage study billing.
Perform field monitoring of clinical trials to ensure data consistency and compliance with GCP and regulatory requirements. Provide oversight of trial activities, mentor junior staff, and contribute to the development of clinical protocols and informed consent forms.
Lead field monitoring and data collection for complex clinical trials while ensuring compliance with GCP and regulatory requirements. Provide strategic direction, mentor junior staff, and oversee trial conduct including metrics and protocol deviations.
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