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Clinical Operations manages and monitors the clinical trial process from study start-up to closeout. All departments within Clinical Operations work collaboratively and cross-functionally to ensure successful study execution.

IT innovates our software solutions, modernizes our infrastructure, and enhances user experiences. Our Software Development team builds proprietary applications across the enterprise, while our IT Infrastructure group supports a global network.

Finance is a corporate function that supports Medpace as a global, publicly traded company. This team is split into multiple departments that focus on analysis, reporting, budgeting, forecasting, and closing activities.

Medpace global laboratory services include routine safety testing, biomarker analysis, bioanalytical services, imaging services, after-bioanalytical services, and more. Positions range from hands-on bench work to detailed project management.

The Regulatory Affairs department is responsible for obtaining approval to initiate clinical trials and for new products and ensuring that approval is maintained. It serves as the interface between the regulatory authority and the project team.

Biometrics is the functional area responsible for collecting, cleaning, and analyzing the data collected at Medpace’s sites and the systems used to collect it. It is an essential Medpace service that ensures that accurate results are presented to our sponsors and other agencies.

Commercial Operations is the liaison between the sponsor and all business-related functions at Medpace. Each department within this functional area plays a critical role in both the bid process and the management of awarded contracts for clinical trials.

Clinical Safety is responsible for the intake and processing of adverse and serious events in clinical trials and post-market surveillance. The department is looking for any patient reactions that may arise in correlation to the therapeutics that we are studying and researching.

Business Development provides essential contributions to the continued growth and success of Medpace by offering high levels of customer support to both new and existing clients and communicating both the scientific and operational benefits of Medpace services to prospective clients.

The Medical Department consists of our Medical Directors and Safety Physicians who are responsible for providing medical, scientific and strategic leadership for successful planning, execution and reporting of clinical trials. They serve as the internal medical expert and as a medical resource for all aspects of the study process.