Research Assist is a contract research organization (CRO) providing clinical trial management services in the area of project development (e.g., protocol writing, IDB development, IND application, selection of vendors, identification of sites, etc.), project implementation (e.g., site qualifications, contract negotiations, conduct investigator meetings, regulatory document review, site initiations, etc.), clinical trial management (e.g., management of site activities, monitoring and tracking of study specific safety and efficacy data, processing of SAE reports, etc.), monitoring, data management, medical writing, clinical pharmacology and regulatory support.

Why RAI? We have a solid infrastructure and a core team of experienced and well qualified professionals to support our efforts in conducting phase 1-4 clinical trials. Each of our core member has greater than 15 years of industry experience, most greater than 20 years managing global clinical trials. With this level of experience, our clinical trials are individually managed with oversight of every detail. The end result is an efficiently run clinical trial, decreased queries and a rapid database lock. Our customers return to us, because they have gotten used to a level of quality they know we will always deliver.