Adjuvant Research Services is a clinical operations services firm providing study planning, study management, clinical trial monitoring as well as trial rescue services to emerging life science companies developing new products for the oncology and vision care markets.
Our offices are located in Newark, Delaware and Manchester, England. Our regional monitors are well positioned nationally to minimize travel time as well as travel expenses.
New drug and device development is challenging. Developing new cancer drugs is particularly difficult, however. Drugs in development for cancer indications experienced the lowest clinical trial success rate of all therapeutic areas since 2004*. Clinical trial design and low accrual rates are cited commonly as reasons for failure. Complicated clinical trials requiring difficult to recruit patient populations will continue to struggle without meticulous site selection,study planning and creative ongoing site management initiatives.
Investing time and resources prior to study initiation is critical to preserve project timelines and data integrity.
Vision CareLeveraging lessons learned from rescuing hundreds of struggling clinical trials, Adjuvant will work with your team using our signature Study PREP program. The right people and right processes for your clinical trial are the most effective drivers of clinical trial efficiency.
|Study Planning||Study Management||Study Monitoring|
|Protocol Optimization||Project Management||Site Visits|
|Site Feasibility||Speedy Study Initiation||Site Engagement|
|Study Awareness||Contract/Budgets||Accrual Management|
|Patient ID/Education||Vendor Management||Site Training|
|Accrual Process Planning||Screening/Randomization||Report Writing|
Develop a strategy for clinical trial success
Sponsors investing in planning,start-up support and careful progress tracking will increase enrollment rates and decrease enrollment time.
Strategic site selection and planning activities along with enrollment validation assessment allow study teams to obtain objective evidence to guide their decision making.
Setting up an investigational site for success is a function of understanding their traning needs and creating practical ways to translate the protocols into practice.
Getting the right subjects starts with understanding the patient pathway and how patients will navigate throught the healthcare system to learn about and utlimately become enrolled in the trial.