Stiris Research
Clinical research organization offering end-to-end clinical development support for biotech and pharmaceutical sponsors. Services emphasize patient-centric protocol review, site advocacy and relationship management (many team members with site-level experience), flexible/scalable resourcing, and operational support across study start-up, monitoring, data management and regulatory activities.
Industries
Nr. of Employees
small (1-50)
Stiris Research
Products
Full-service Clinical Trial Management CRO
Stiris Research Inc. provides comprehensive study management solutions for Phase I through Phase IIIB clinical research, offering tailor-made services from full-service outsourcing to focused clinical trial management.
Project Rescue Clinical Trial Management Service
A specialized service by Stiris to manage and rescue clinical trials that are jeopardized due to recruitment lags, monitoring issues, data quality problems, or site relationship challenges. The service includes designing and implementing rescue strategies to get trials back on track.
Project Management Services
Comprehensive project management for clinical trials including budget management, team coordination, risk management, and proactive study oversight by experienced project managers.
Clinical Monitoring Services
Clinical Research Associates (CRAs) manage and monitor clinical trial sites to ensure recruitment, data quality, and issue management meet study goals.
Medical Monitoring and Pharmacovigilance Services
Comprehensive medical affairs and pharmacovigilance services including 24/7 medical monitoring, SAE management, safety data review, and medical review of clinical documents.
Biostatistics and Data Management Services
Data management and biostatistics support for clinical trials including early phase, pivotal, and late phase studies with rapid execution and personalized service.
Full-service Clinical Trial Management CRO
Stiris Research Inc. provides comprehensive study management solutions for Phase I through Phase IIIB clinical research, offering tailor-made services from full-service outsourcing to focused clinical trial management.
Project Rescue Clinical Trial Management Service
A specialized service by Stiris to manage and rescue clinical trials that are jeopardized due to recruitment lags, monitoring issues, data quality problems, or site relationship challenges. The service includes designing and implementing rescue strategies to get trials back on track.
Project Management Services
Comprehensive project management for clinical trials including budget management, team coordination, risk management, and proactive study oversight by experienced project managers.
Clinical Monitoring Services
Clinical Research Associates (CRAs) manage and monitor clinical trial sites to ensure recruitment, data quality, and issue management meet study goals.
Medical Monitoring and Pharmacovigilance Services
Comprehensive medical affairs and pharmacovigilance services including 24/7 medical monitoring, SAE management, safety data review, and medical review of clinical documents.
Biostatistics and Data Management Services
Data management and biostatistics support for clinical trials including early phase, pivotal, and late phase studies with rapid execution and personalized service.
Services
Intervention and remediation for underperforming studies, including rapid team deployment and post-rescue monitoring.
Full project management of clinical studies, providing a consistent core team through study conduct to data lock.
On-site and remote monitoring services to ensure protocol compliance and data integrity.
Services to accelerate site selection, initiation and activation to improve enrollment timelines.
Clinical safety oversight and medical review services during study conduct.
Audit services to assess compliance with protocol and regulatory standards.
Intervention and remediation for underperforming studies, including rapid team deployment and post-rescue monitoring.
Full project management of clinical studies, providing a consistent core team through study conduct to data lock.
On-site and remote monitoring services to ensure protocol compliance and data integrity.
Services to accelerate site selection, initiation and activation to improve enrollment timelines.
Clinical safety oversight and medical review services during study conduct.
Audit services to assess compliance with protocol and regulatory standards.
Expertise Areas
- Clinical trial management
- Clinical monitoring (on-site and remote)
- Study start-up and site activation
- Patient engagement and decentralized trials
Key Technologies
- Clinical Trial Management Systems (CTMS)
- Electronic Trial Master File (eTMF)
- Remote/central monitoring platforms
- Clinical data management and interim analysis workflows
News & Updates
Conference attendance at DPHARM (conference focused on innovation in clinical trials).
Participation in an invitation-only forum for pharma and biotech executives to discuss clinical trial execution and efficiencies.
Attendance at the CNS Summit, bringing together decision makers across pharma, biotech and clinical research.
Perspective article reflecting on regulatory conference insights and patient-focused approaches.
Perspective on oncology advances and implications for clinical operations.
Conference reflection discussing insights and actions for clinical research.
Conference attendance at DPHARM (conference focused on innovation in clinical trials).
Participation in an invitation-only forum for pharma and biotech executives to discuss clinical trial execution and efficiencies.
Attendance at the CNS Summit, bringing together decision makers across pharma, biotech and clinical research.
Perspective article reflecting on regulatory conference insights and patient-focused approaches.
Perspective on oncology advances and implications for clinical operations.
Conference reflection discussing insights and actions for clinical research.