NOVA Research Company performs a wide range of clinical research services, from developing research applications and protocols, to developing all the necessary clinical materials to carry out the research and preparing IRB packages for approval. Our team implements research programs for both single-site and multi-site studies, conducts research, analyzes data, and develops research findings and conclusions. NOVA also creates presentations, develops peer-reviewed publications and disseminates the results including both U.S. and international research.
Our clinical research team provides the following expertise and services:
Developing research applications and clinical research materials
Implementing research programs, conducting research and data analysis, and developing conclusions
Developing publications and disseminating results
Performing R01 and R03 research studies
Providing research and support services to outside investigator-conducted research
Our clinical research services team has experience with an array of services, from developing initial research protocols, to preparing findings, publications, and conclusions to complete your study.
For more information on our clinical research services, please contact Paul Young at 301-986-1891, Ext.110 or .
Development of an Adolescent HIV/STD Risk-of-Exposure Screen Instrument
The goal of this 5-year NIH-funded study is to develop a valid, brief adolescent-appropriate screen for HIV/STD risk configured like the widely used 10-scale POSIT (Problem Oriented Screening Instrument for Teenagers) questionnaire. Read more.
Research Subject Recruitment, Screening, Evaluation, Discharge, and Follow-Up Services for the NIDA Intramural Research Program (IRP)
Since 1991, NOVA has provided clinical research support services to NIDA's IRP. Read more.
Clinical Trials Support to the National Institute of Neurological Disorders and Stroke (NINDS)
NOVA staff provided research support from initial assistance with study design, clinical record forms design, database design, and identification of appropriate study endpoints through implementation of case-control data collection forms, conduct of data collection, quality control, formation of and facilitation for logistics of patient data and safety monitoring committees and providing clinical coordinations to assist investigators with technical and administrative conduct of clinical trials. Read more.