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

biotechnology
clinical-trials
pharmaceutical
project-management-db17

Nr. of Employees

small (1-50)

Stiris Research


Products

Clinical Trial Management

Comprehensive management of clinical trials including site identification, feasibility, startup, monitoring, and data management to support biotech and pharmaceutical studies.

Rescue Project Management

Intervention service to recover and realign clinical trials facing challenges such as recruitment delays, monitoring issues, or damaged site relationships.

Project Management

Leadership and coordination of clinical trial activities including budget management, team coordination, risk mitigation, and communication facilitation.

Clinical Monitoring

Site management and monitoring services to ensure compliance, data quality, and patient safety throughout clinical trials.

Medical Monitoring

Medical oversight and pharmacovigilance services including safety monitoring, adverse event management, and medical review of clinical documents.

Auditing and Compliance Consulting

Auditing services and compliance consulting to assess and improve adherence to regulatory standards and quality management systems.


Services

Rescue services

Intervention and remediation for underperforming studies, including rapid team deployment and post-rescue monitoring.

Project management

Full project management of clinical studies, providing a consistent core team through study conduct to data lock.

Clinical monitoring

On-site and remote monitoring services to ensure protocol compliance and data integrity.

Study start-up

Services to accelerate site selection, initiation and activation to improve enrollment timelines.

Medical monitoring

Clinical safety oversight and medical review services during study conduct.

Auditing

Audit services to assess compliance with protocol and regulatory standards.

View All Services

Expertise Areas

  • Clinical trial management
  • Clinical monitoring (on-site and remote)
  • Study start-up and site activation
  • Patient engagement and decentralized trials
  • Show More (4)

Key Technologies

  • Clinical Trial Management Systems (CTMS)
  • Electronic Trial Master File (eTMF)
  • Remote/central monitoring platforms
  • Clinical data management and interim analysis workflows
  • Show More (1)

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