Clinovative Research Inc (CRI) is a contract research organization providing clinical trial management, monitoring, medical writing, auditing, and training services to clients and partners in pharmaceutical, medical device, biotechnology, academic, and government organizations.  With a home office near Research Triangle Park in North Carolina, we boast staff and CRAs located throughout the United States to ensure cost-effective and timely service to our clients. 

As one of the smaller CROs, our organization can remain client focused and nimble, allowing us to provide high-quality data with low overhead costs and quick response times.  Being small does not limit our abilities, however.  We possess many of the benefits of larger companies, including the capability and experience to conduct investigator-initiated trials, large international trials, and those in between. 

Our staff is highly skilled and has great diversity of experience, with each CRA holding an RN, BS, or MS and having at least 3 years of clinical research experience.  We provide ample training and conference opportunities for our staff in order to provide you with a well-educated and informed team who are knowledgeable about the therapeutic area, all applicable clinical trial regulations, and patient population prior to the start of your study.  In addition, we have a low attrition rate for CRAs which enhances our ability to remain consistent and effective when executing clinical trials.  Most of our staff has worked on both INDs and IDEs and understand the regulatory nuances of various product types. 

CRI has worked in a wide-range of therapeutic areas, including oncology, gastroenterology, cardiology, respiratory/pulmonary, rheumatology, and hematology.  We have also worked with orphan drugs, pediatric indications, and apheresis trials.  With our client-centered focus and flexibility, we can manage your clinical trial from inception to submission or augment ongoing CRO/CRA activities by bolstering site/subject recruitment, speeding up the regulatory phase, or providing additional monitoring, rescue monitoring, or oversight services.   

For investigative sites, we offer a variety of training options for investigators and coordinators that will help you maximize your resources, meet your regulatory obligations, and minimize cost.  These include clinical coordinator training or refresher training, assistance with regulatory file set up or systems management, subject recruitment assistance, or IRB submission assistance.   We also offer independent audit services and FDA/IRB audit-prep services. 

Whatever your clinical trial needs, Clinovative is committed to providing you with innovative solutions that will maximize your clinical trial.