CARE is looking for new physician partners in and beyond the Pacific Northwest.
Partnering with CARE
Benefits to Your Practice
Increased revenue and equity interest through a Joint Venture partnership with CARE
Opportunity to offer alternative therapies to patients
Positions your practice at the forefront of new patient therapies
Coordination of Clinical Trials
CARE Manages all aspects of the clinical trial by providing experienced clinical research coordinators that ensure proper subject consent, medical histories, lab draws, vitals, etc. are all performed according to the protocol and at the direction of the Principal Investigator
CARE resolves all data queries, oversees monitoring and audit visits required by the FDA and ensures proper investigational product and device accountability.
CARE handles all shipping of lab samples and other hazardous materials.
CARE uses CRIO research software for all study documentation giving Investigators complete oversight of their trials no matter where they are.
CARE Institute administers all regulatory procedures including submission to the Institutional Review Board (IRB), protocol training implementation and documentation, ongoing regulatory maintenance and closeout of study documentation at the end of each protocol. We use CRIO’s state-of-the-art eRegulatory Documentation software.
Contracts and Budget
All contracts (Confidentiality Agreements, Clinical Trial Agreements, etc.) and budgets are negotiated by a Certified Clinical Research Contracts Professional (MAGI). Additionally, a contract attorney is maintained on retainer for any necessary consultations regarding contract language or implementation.
We utilize CRIO’s Clinical Trial Management Software program to manage all study payments both from study sponsors as well as to vendors, physicians and subjects for subject visit stipends.