Clinical Operations

Case:  Mid-sized pharma company, fully outsourced, heavily reliant on spreadsheets to manage trials 

Transparency and visibility into study status across multiple therapeutic areas, regions, countries, sites and other multiple vendors are made more difficult by use of disparate data systems and the lack of adequate internal systems.  Furthermore, lack of a standardized and harmonized information system to capture study metrics hinders the ability to use historic data for study planning & feasibility while also preventing data mining exercises that could drive efficiency. 

The platforms developed can put study teams in a better position to deliver studies in a timely and cost effective manner by having the ability to actively manage global trials and to quickly identify quality sites by therapeutic area for upcoming trials based on past experience 

Provides data enabling better understanding of geographical footprint, startup cycle times by country, ability to choose study locations in order to accelerate patient recruitment, and compare trial management factors such as data quality and site management. 

Additional Information

OPTIMIZING SITE PERFORMANCE	OPTIMIZING PATIENT RECRUITMENT	ACTIVE STUDY MANAGEMENT
SITE SURVEILANCE	IMPROVE STUDY CLOSE	VENDOR MANAGEMENT
INVESTIGATOR DATABASE W/ PERFORMANCE METRICS