Aris Clinical
Aris Clinical, established in 1999, specializes in clinical research management with a focus on delivering successful clinical trials across various therapeutic areas. They emphasize risk management, flexibility, and detailed attention to client needs, aiming to bring projects to completion on time and with optimal results. Their expertise spans from trial inception to rescue, with a dedicated team of highly qualified professionals committed to quality and success.
Industries
Nr. of Employees
small (1-50)
Products
Project Rescue
Targeted intervention and management services designed to rescue troubled, delayed, or derailed clinical trials.
Study Management
Coordination of all aspects of the trial process including budget development, timeline creation, status reporting, vendor management, and communications.
Monitoring and Site Management
Clinical Research Associates (CRAs) evaluating and selecting sites, assisting with site management, and making critical decisions for clinical trials.
Clinical Operations Management
Operational oversight for study teams or departments to ensure quality, productivity, and efficiency while meeting client objectives, including budget and timeline management, SOP development, and vendor contract negotiations.
Centralized Data Review
Centralized review of study data utilizing data listings, patient profiles, EDC, and other data sources to identify issues and achieve data quality for milestones.
Flexible Staffing Solutions
Personnel support for variable workload and talent needs, including virtual, regional, and on-site options from start-up to closeout.
Project Rescue
Targeted intervention and management services designed to rescue troubled, delayed, or derailed clinical trials.
Study Management
Coordination of all aspects of the trial process including budget development, timeline creation, status reporting, vendor management, and communications.
Monitoring and Site Management
Clinical Research Associates (CRAs) evaluating and selecting sites, assisting with site management, and making critical decisions for clinical trials.
Clinical Operations Management
Operational oversight for study teams or departments to ensure quality, productivity, and efficiency while meeting client objectives, including budget and timeline management, SOP development, and vendor contract negotiations.
Centralized Data Review
Centralized review of study data utilizing data listings, patient profiles, EDC, and other data sources to identify issues and achieve data quality for milestones.
Flexible Staffing Solutions
Personnel support for variable workload and talent needs, including virtual, regional, and on-site options from start-up to closeout.
Services
Operational oversight for study teams or departments, including SOP development, budget and timeline management, and vendor contract oversight.
Assessment of client capabilities and trial requirements to recommend appropriate outsourcing strategies and partners.
Provision of clinical monitoring services including site selection, initiation, monitoring visits, and closeout; emphasis on experienced clinical research associates.
Provision and management of personnel to support variable workload and specialized talent needs using virtual, regional, and on-site staffing models.
Project management services spanning study start-up, timeline and budget management, vendor coordination, and status reporting acting as the primary point of contact for sponsors.
Intervention services to identify and correct operational and design issues in underperforming or delayed clinical trials to restore progress and meet milestones.
Operational oversight for study teams or departments, including SOP development, budget and timeline management, and vendor contract oversight.
Assessment of client capabilities and trial requirements to recommend appropriate outsourcing strategies and partners.
Provision of clinical monitoring services including site selection, initiation, monitoring visits, and closeout; emphasis on experienced clinical research associates.
Provision and management of personnel to support variable workload and specialized talent needs using virtual, regional, and on-site staffing models.
Project management services spanning study start-up, timeline and budget management, vendor coordination, and status reporting acting as the primary point of contact for sponsors.
Intervention services to identify and correct operational and design issues in underperforming or delayed clinical trials to restore progress and meet milestones.
Expertise Areas
- Clinical trial management
- Clinical operations
- Monitoring and site management
- Study management
Key Technologies
- Electronic data capture (EDC)
- Centralized data monitoring and review
- Clinical trial management systems (CTMS)
- Remote/virtual staffing platforms