Medpace is a scientifically-driven, global, full-service clinical contract research organization (CRO) providing Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries.

Research

Medpace

Medpace's headquarters in Cincinnati, OH, United States

August Troendle

Susan Burwig

Stephen Ewald

Tracy Miller

Miaesha Campbell

Carolyn Glashagen

Reinilde Heyrman

Brandon Ebken

Kevin Brady

Todd Meyers

The Leadership Team at Medpace is responsible for setting the strategic direction and overseeing the execution of clinical development services across the organization. This team, comprised of senior executives from various domains such as operations, medical affairs, compliance, and finance, collaborates to ensure the successful delivery of Phase I-IV clinical trials, uphold quality standards, and drive business growth while managing risk and regulatory compliance in the biotechnology and pharmaceutical sectors.

Leadership Team

The Clinical Research Team at Medpace is responsible for overseeing and managing the execution of clinical trials across various phases, ensuring compliance with regulatory standards and protocols. This team comprises Clinical Research Associates and Senior Clinical Research Associates who work collaboratively to monitor study sites, collect and analyze clinical data, and facilitate communication between stakeholders, contributing to the successful development of new medical treatments and therapies. Their expertise ensures that clinical trials are conducted efficiently and ethically, ultimately advancing the healthcare landscape.

Clinical Research Team

The Data Management and Analysis Team at Medpace is responsible for overseeing the collection, management, and analysis of clinical trial data to ensure its integrity and compliance with regulatory standards. This multidisciplinary team collaborates with various stakeholders to develop and implement data management strategies, optimize data processing workflows, and leverage advanced analytics to support decision-making throughout the clinical trial lifecycle. Their efforts are crucial in delivering high-quality data that drives successful clinical outcomes for clients in the biotechnology and pharmaceutical industries.

Data Management and Analysis Team

The Medical Writing and Regulatory Affairs Team at Medpace is responsible for creating high-quality regulatory documents and ensuring compliance with industry standards. This team collaborates closely with clinical researchers and regulatory authorities to draft protocols, clinical study reports, and submission materials that facilitate the approval process of new drugs and devices. Their expertise ensures that all written materials clearly communicate scientific data and adhere to regulatory guidelines, supporting Medpace's mission to advance clinical development in the biotechnology and pharmaceutical sectors.

Medical Writing and Regulatory Affairs Team

The Information Technology and Development Team at Medpace is responsible for designing, developing, and maintaining innovative software applications and IT infrastructure that support clinical trial operations. This team collaborates cross-functionally to ensure the reliability, scalability, and security of technological solutions, enhancing the efficiency of clinical development services across the organization. Their expertise in software engineering, network management, and system validation is critical for advancing Medpace's mission in the biotechnology and pharmaceutical sectors.

��

Medpace

Org chart

Teams

Leadership Team

Clinical Research Team

Data Management and Analysis Team

Medical Writing and Regulatory Affairs Team

Information Technology and Development Team

Offices

��������

Medpace

Org chart

Teams

Leadership Team

Clinical Research Team

Data Management and Analysis Team

Medical Writing and Regulatory Affairs Team

Information Technology and Development Team

Offices

Related companies

��