Expertise embedded in trials – throughout the project lifecycle
One Team – One Approach
Engage with one cross-functional team that actively participates in your trial or program – from early planning through close-out. Our approach maintains continuity and optimizes performance while building strong team chemistry, minimizing disruptions, and ensuring high-quality results across our full breadth of services. With deep scientific and therapeutic expertise, our teams are poised to lead the industry’s most innovative and challenging clinical trials.
Expertise embedded in trials – throughout the project lifecycle
One Team – One Approach
Engage with one cross-functional team that actively participates in your trial or program – from early planning through close-out. Our approach maintains continuity and optimizes performance while building strong team chemistry, minimizing disruptions, and ensuring high-quality results across our full breadth of services. With deep scientific and therapeutic expertise, our teams are poised to lead the industry’s most innovative and challenging clinical trials.
Study Strategy
Medical
Operations
Regulatory Affairs
Biometrics
Clinical Informatics & Feasibility
Labs
Imaging
Optimize your development strategy with insights and guidance from experts across Medpace.
Study Execution
Regulatory Services
Study Start-Up
Clinical Trial Management
Vendor Management
Clinical Packaging & Supplies
Patient Recruitment & Retention
Clinical Monitoring
Data Management
Biostatistics
Medical Monitoring
Safety & Pharmacovigilance
Endpoint Adjudication
Independent Data Monitoring Committee (IMDCI)
Medical Writing
Quality Assurance
Account Management
Integrated Services
Central Labs
Bioanalytical Labs
Imaging Core Labs
Cardiovascular Labs
Phase I Unit
Even the most complex study designs are streamlined by working with a single vendor with the expertise and staffing needed to collect and analyze critical endpoints.
Technology
Clinical Trial Management System
Electronic Data Capture (EDC)
ePRO / eCOA / eDiary / eConsent
Interactive Response Technology (IRT)
ClinTrak Data Explorer
Centralized Monitoring
eTMF
Wearables
Imaging Management
TrialPACE Patient App
OnPACE Site App
Lab Information
Management System (LIMS)
“In an increasingly complex drug development environment, direct access to scientific expertise is indispensable. Our experts are embedded in your projects and go well beyond executing to specs—they work directly with your team to map our the best course of action. This drives quality and avoids missteps that could cost time and money.”
Traci Turner, MD, MT (ASCP) Vice President of MRL Operations & MARC, Medpace
Our Talent – Your Advantage
At Medpace, excellence isn’t just a goal—it’s ingrained in our DNA. Our teams boast top-tier talent, from MDs with deep industry and clinical experience to specialized Clinical Trial Management experts and PhD-level scientists. With a focus on ongoing training and development, we cultivate cohesive, high-performing, accessible teams that deliver unparalleled results.
Rely on our high-science organization’s caliber of talent and expertise to enhance your clinical development journey, backed by our unwavering commitment to driving the highest quality performance.
Integrated Services and Capabilities
Streamline even the most complex clinical trials with a full-service, single-vendor outsourcing strategy. Our comprehensive CRO services are supported by our wholly-owned Central Laboratories, Bioanalytical Lab, Imaging Core Lab, ECG Core Lab, and Phase I Unit, as well as a Clinical Trial Management System that ties all study data together in a single platform. With integrated services and systems, we achieve higher levels of efficiency and productivity.
