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Overview Established in 1992, Medpace has partnered with leading pharmaceutical and biotech companies to bring promising new drugs to market. Medpace combines efficient clinical trial management with comprehensive regulatory consulting to provide Sponsors with exceptional support during the drug development process.

The integrated services at Medpace include: clinical development plan preparation, project management, regulatory document preparation, safety surveillance, clinical monitoring, data management, statistical analysis, medical writing, quality assurance auditing, and US and international regulatory submissions.

At Medpace, proven leaders in medical and scientific research monitor every project. The therapeutic focus and experience of the Medpace team, which includes on-staff physicians, reduces the need for client oversight, review, and training. In addition, Medpace physicians have first-hand experience working with regulatory agencies to successfully guide projects through the complexities of the regulatory process. The medical expertise and regulatory guidance provided by Medpace leads to reduced costs and increased efficiencies for our valued customers.

Medpace brings together an exceptionally well-qualified team of medical and scientific personnel for every project. This team-based approach, combined with comprehensive training programs, active career development and cross-training opportunities, has significantly reduced attrition. This provides Sponsors with personalized service and the potential for long-term partnerships.

Medpace offers a variety of leading edge technologies to track, interpret, and communicate information in the most timely, secure, and cost-effective manner. ClinTrak®, a web-based, proprietary research management system designed by Medpace, offers access to near real-time study data and metrics. 

Jobs at Medpace

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