A TYPICAL PHASE III CLINICAL TRIAL TAKES NINE MONTHS TO COMPLETE ENROLLMENT AND CAN COST UP TO $86 MILLION.
Using our internal databases which contain extensive information based on past experience with sites, our team provides patient qualification, recruiting and appointment scheduling to assure that patient enrollment can support trial parameters in a timely, quality fashion. Our pre-screening processes are designed to facilitate qualification and find the best patient fit for each study while allowing your research coordinators to maximize their skills and time by allowing them to focus on their patients.
|Increase scheduled appointments|
|Increase patients that achieve randomization|
|Increase your in house staff efficiencies|
|Increase patient interaction|
|Decrease no show rates|
Technology enabled recruitment
WE USE INTRANET SITES TO HOUSE STUDY DETAILS & THEIR INCLUSION AND EXCLUSION CRITERIA WE HAVE HEALTH-FOCUSED ONLINE SOCIAL COMMUNITIES FORMED AROUND SPECIFIC MEDICAL CONDITIONS WE USE SOCIAL MEDIA TO EDUCATE POTENTIAL PATIENTS ABOUT THE VALUE OF CLINICAL RESEARCH & ENCOURAGE THEM TO PARTICIPATE. WE USE MOBILE DEVICES TO DISSEMINATE INFORMATION TO PATIENTS.
|Input and update all new and existing patient records|
|Handling both inbound response and outbound calls|
|Gather candidate information for future trials|
|Conduct reminder calls for pre-appointment instructions|
|Sending directions and prepare candidate for initial screen|
|Manage data filters for optimizing database searches in CTMS|
|Set up programs within CTMS to track marketing efforts|