Experience
TrialAssist services are provided by expert staff that have extensive experience in all phases of study organisation from protocol and CRF design and regulatory approvals through “in study” management and recruitment advice to data handling and report writing.
TrialAssist staff can help and support investigators to undertake study sponsors' responsibilities from planning to publication, with contracts in place between the Investigator and TrialAssist.
TrialAssist will not interfere with the valuable relationship between investigator and pharmaceutical company, but will help to safeguard the investment made by both parties (in time and money) and allow the IST “hands off ”approach required of the company.
TrialAssist will work to ensure that you achieve productive, cost effective Investigator Sponsored Trials that produce publishable results.