Vacatures Medpace Medical Device B.V.
Vaals
Contract Research Organization
The advantage of Medpace.
A global leader in research-based drug and medical device development, Medpace builds strong strategic partnerships with select Sponsors to advance the most efficient and cost-effective path to approval. As a therapeutically-focused Contract Research Organization (CRO), we view ourselves as stewards of your drug and device, leveraging our extensive medical and regulatory expertise to deliver additional input, strategy, and efficiencies to each and every phase of the clinical trial. Medpace has the breadth, depth, and flexibility to deliver a superior result, specific to your needs, on six continents.
The advantage of expertise.
Led by top therapeutic, regulatory and operational experts with extensive experience in the advancement of pharmaceutical agents and medical devices, Medpace has cultivated a culture of expertise. Following our unique partnering philosophy, our dedicated teams serve as an extension of your team, ensuring unmatched execution from start to finish. Before we even begin a trial, the Medpace proactive industry experts are already working on the right answers to streamline your development process and accelerate time to product approval.
The advantage of global reach.
Medpace is a privately held company headquartered in Cincinnati, OH with offices and laboratories throughout Europe, Asia, the Middle East, Australia, Africa, and the Americas. Our expanding global reach is interconnected through an innovative suite of proprietary technologies, ClinTrak, a study management system facilitating team coordination and providing decision support for sponsors and sites, to ensure global teams are focused and organized for maximum efficiencies using a common data platform. Clintrak provides near real time access to critical study data, including lab and imaging information pertaining to the study.
The advantage of focus.
For over 20 years, Medpace has adhered to a full-service contract research model. Our disciplined approach to trial execution engages our medical, regulatory and operational teams to perform delivers higher quality results in the most timely and efficient manner. Coordinating all resources and services provides an accountable, seamless, integrated and efficient platform increasing quality and speed while significantly reducing a Sponsors need for duplicate management oversight.
