Services

Sponsors & CROs

Clinnova Research Solutions is a full-service SMO that provides administrative and operational support to help facilitate Phase II-IV clinical trials. We conduct research in high-quality, fully equipped facilities located in Orange and Torrance, California. By utilizing our extensive network of experienced investigators, patient access, and research expertise, we can conduct our clinical trials ethically and efficiently, with minimal deviation.

Let us see how we can help you reach your study goals.

Clinnova Research Solutions currently offers investigational sites in Orange and Torrance, California. At each location we offer experienced research coordinators and accomplished investigators whom you can rely on for your project needs. All coordinators and supporting site staff are properly trained to manage the clinical research operations while maintaining the highest standards in regulatory and safety protocol adherence and in ICH-GCP compliance.

Budget planning and negotiations
Data analytics and management
Oversight of site-specific quality and safety metrics
Clinical training for research coordinators and supporting site staff
Site initiation, activation, and close-out operations

Investigational Sites

Sponsors & CROs

Clinnova Research Solutions is a full-service SMO that provides administrative and operational support to help facilitate Phase II-IV clinical trials. We conduct research in high-quality, fully equipped facilities located throughout the Orange County area of Southern California. By utilizing our extensive network of experienced investigators, patient access, and research expertise, we can conduct our clinical trials ethically and efficiently, with minimal deviation.

Let us see how we can help you reach your study goals.

Investigational Sites

Each investigational site offers experienced research coordinators and accomplished investigators whom you can rely on for your project needs.

Staffing and Recruiting:

Clinnova manages the recruitment and hiring of clinical research coordinators, phlebotomists, and other supporting staff. During onboarding, all new staff are properly trained to manage paper and digital-based clinical research operations while maintaining the highest standards in regulatory and safety protocol adherence as well as ICG-GCP compliance.

Our Investigational Sites Also Include:

Budget planning and negotiations
Data analytics and management
Oversight of site-specific quality and safety metrics
Site initiation, activation, and close-out operations