About Guardian Research
Mission of Guardian Research
The core mission of Guardian Research is to develop and continuously build upon a clinical trials center of excellence that promotes active involvement of community based providers and their patients in timely clinical research dedicated to discovering new and life changing therapies, optimizing medical practice, and advancing health locally.
Mission of Guardian Research
The core mission of Guardian Research is to develop and continuously build upon a clinical trials center of excellence that promotes active involvement of community based providers and their patients in timely clinical research dedicated to discovering new and life changing therapies, optimizing medical practice, and advancing health locally.
Mission of Guardian Research
The core mission of Guardian Research is to develop and continuously build upon a clinical trials center of excellence that promotes active involvement of community based providers and their patients in timely clinical research dedicated to discovering new and life changing therapies, optimizing medical practice, and advancing health locally.
- Steadfast adherence to a moral compass that is firmly directed at engaging in clinical research that fosters improved patient experience of care and improved health of populations.
- Generating breakthroughs and innovations in transforming health and health care.
- Continuous promotion of transparency, compliance, and accountability in clinical research endeavors.
- Protecting information integrity, patient privacy, and security, through full compliance with State and Federal privacy and security regulations, and regulations guiding clinical trials.
- Building collaborative relationships and shared success among and between community-based providers.
- Stimulate broad-based involvement of community based providers in clinical trials and the advancement of medical science and treatment alternatives.
- Engagement of a clinical research support team dedicated to facilitating timely activation and administration of clinical trials.
- Continuous training of research support staff.
- Maintenance of a centralized web-based repository of clinical trials protocol-specific documents and consents.
- Clinical research information systems management.
- Recruitment, screening and enrollment of clinical trial specific eligible patients.
- On-going internal review and auditing to ensure a high level of clinical trial specific data accuracy and integrity.
- Systematic monitoring clinical trial protocol compliance.
- Comprehensive adverse event reporting.
- Coordination of patient treatment on research study.
- Dedicated commitment to quality assurance through organization wide adherence to a comprehensive quality assurance and compliance program.