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Risk Based Monitoring - A CRO Perspective

Risk Based Monitoring - A CRO Perspective

Dr. Alex Artyomenko addresses the need to coordinate and collaborate across functions within both the Sponsor and CRO organizations to breed success when implementing an RBM approach.
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Planning and Executing a Clinical Study for an Orphan Indication

Clinical Research in Orphan Indications

Planning and executing a clinical study for an orphan indication presents a unique set of challenges and considerations. In this 30-minute presentation learn successful strategies and best practices for addressing some of these.
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Do you have what it takes to be a member of our team?

Medpace is not just another CRO. We have a disciplined approach to drug and medical device development that requires passionate people who want to excel. Want to talk? Check out these Career Opportunities

Integrated study design at early stages can set the stage for study efficiency and success at later phases. Medpace Early Stage teams provide the newest innovations in bench to bedside techniques, supporting success early on. LEARN MORE Learn more about early phase clinical development
Medpace teams that can engage quickly and provide strategic thinking at every phase of trial are critical for study success. Therapeutically focused study teams bring energy, expertise, and commitment to every phase of the drug development process. LEARN MORE Learn about Phase II - II clinical development
LABS labs
Key support providing consistency in methods and instrumentation on a global stage are critical to support fully integrated studies. Medpace provides core laboratory capabilities supported across 40 countries for truly stellar performance. LEARN MORE Learn about Medpace Labs
Medpace offers a fully-dedicated and specialized division for the design and conduct of medical device trials. Led by clinical and regulatory experts located in the US and Europe, Medpace is uniquely qualified to accelerate the approval of your medical device. LEARN MORE Learn about Medpace Medical Device CRO
The pathway to success in bringing compounds and devices to regulatory approval requires integrated study teams across the globe. Medpace delivers study excellence on six continents through best-in-class, global experts to manage your next project. LEARN MORE Learn more about Medpace CRO and our global capabilities
careers Careers
Medpace is the place to be for industry experts who care about succeeding in the life science arena. We are committed to providing you with opportunities to learn and develop. We view your success as an investment in our future.

investigators Investigators
Partnering with Medpace as an investigator is a rewarding experience. Medpace prides itself on creating a partnership with the best study sites providing support for the development of innovative therapeutics. Join our team.

sign up Study Participants
Medpace CPU conducts early phase clinical research studies. Our purpose is to carry out high-quality medical research. Our goal is to advance medical knowledge and help bring new drugs to the public. By participating in clinical studies you can help find cures for many diseases.

March 24 - 25, 2015
4th Annual Outsourcing in Clinical Trials Southeast
Cary, US

March 24 - 28, 2015
AAOS Annual Meeting
Las Vegas, US

13 - 15 April 2015
DIA EuroMeeting
Paris, FR

April 14 - 16, 2015
Innovation in Medtech
Dublin, IE

April 14 - 16, 2015
SQA Annual Meeting
Tampa, US

April 15 - 16, 2015
Clinical Operations in Oncology Trials West Coast
Burlingame, US

April 22 - 24, 2015
Partnerships in Clinical Trials
Boston, US

25 - 28 April 2015
Copenhagen, DK

April 25 - 28, 2015
ACRP 2015 Global Conference & Exhibition
Salt Lake City, US

April 27 - 29, 2015
2015 Diabetes Summit
Boston, US

April 28, 2015
PCMG ARO Workshop
Brussels, BE

April 28, 2015
PCMG ARO Workshop
Brussels, BE


request info Medpace is ready to help you with your next clinical trial project. Find out more about how we can help.

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