Experience has taught us that effective and consistent communication between the Sponsor, investigator and
research sites, patients, and the Clinical Research Organization (CRO) is integral to the success of every
clinical trial. It's a matter of how we think about drug development at Medpace – we recognize that development time is
crucial and we believe that partnering leads to projects being delivered quickly, efficiently, and cost
effectively.
This unique partnering philosophy is what drives us – we know how to successfully manage our partners'
projects and our infrastructure is designed to leverage this knowledge to proactively deliver superior
insight, strategy, and efficiencies to each and every phase of trial. At Medpace, we build long-term
relationships that ensure results.
Sponsor Partnerships
Medpace shares a common goal with our Sponsors – advancing drugs from development plan to regulatory
approval in the most accurate, efficient, and cost-effective manner. Our Sponsors seek a
dedicated partner who
can engage quickly and provide strategic thinking. Every Medpace project team is structured to serve as an
extension of your team. Every partnership is designed to create
research solutions focused on your unique
clinical trial. Led by the industry's top
therapeutic and
regulatory experts,
our proficient and experienced employees are committed to providing you with best in class service and
unrivaled support at every stage of the drug development process. And because we have one of the lowest
turnover rates in the industry, we keep costs down and every project running smoothly and efficiently.
Investigator and Research Site Partnerships
The success of clinical trials is measured in terms of data quality, speed, and cost effectiveness –
Medpace recognizes that partnering with the right investigators to meet recruitment challenges across all
research sites is critical to this success. We know what's most important to investigators – good protocol
design, project planning and organization, and open, effective communication. With medical and regulatory
expertise in drug development in
multiple therapeutic
specialties, we apply our extensive experience working with thousands of investigators and research sites
around the world. Our therapeutically-focused
Clinical Research Associates are dedicated to an average of only two projects at a time so they can
concentrate on process excellence, training research site personnel, and ensuring that
everyone is focused on your unique clinical trial. As a result, we have developed consistent, longstanding,
and positive partnerships with each of our research sites.
Patient Partnerships
Medpace places a high value on study participant relationships. Patient volunteers are essential to the
success of the drug development process, without them it would be impossible to research new medical
treatments that have the potential to improve the quality of life. Led and trained by the top
medical experts in
the industry, Medpace has an uncompromising commitment to the highest level of
ethical standards and safety. We make
sure patients are always treated with respect and consideration and have reliable and accurate information
throughout the study.
Want to learn more? Browse our capabilities, or
contact the location nearest you.