Roles that fit you
Explore Opportunities by Functional Area
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 observes for any patient reactions that may arise in correlation to the therapeutics that are being studied.
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.
QA focuses on compliance to ensure safety of research participants and the integrity, quality, and reliability of data obtained from our clinical trials and labs.
Specifically Designed for CRAs and In-House CRAs
Keeping PACE®
Professionals Achieving CRA Excellence®
Medpace hires both industry experienced professionals as well as individuals new to clinical research. Medpace provides comprehensive and ongoing training for CRAs and In-House CRAs, unmatched by other CROs. Through our PACE Training Program, you will join other Professionals Achieving CRA Excellence. Prepare your CRA skills through interactive discussions and hands-on job-related exercises and practicums. You will have the opportunity to collaborate and network with industry-leading professionals, as you learn aspects of the development and approval process for drugs, biologics, and medical devices.
Commitment to Quality & Compliance
PACE® provides a detailed and thorough training curriculum that includes applicable local regulations, ICH/GCP, Medpace SOPs, specialized departmental trainings, industry best practices, and therapeutic area reviews.
PACE® Monitoring Certificate Programs
As an extension of PACE®, Medpace offers advanced training curricula and on-site field-based and/or remote training trips, to provide CRAs with the necessary skills and experience to monitor complex studies (e.g., Oncology, Cell & Gene Therapy, Rare Disease, Infectious Disease, Neuroscience, Medical Device, Radiopharmaceutical, Phase 1).
Ongoing Development
After completing PACE®, Medpace CRAs continue to receive ongoing training through the monthly CRA newsletter and seminars offered approximately once a quarter, as well as ongoing development by a support network of CRA Managers and project team leaders.
Expand Your Network
Recruitment Events
We host and attend recruitment events throughout the year, globally. Visit the Medpace team and say Hello.
Professional Development
The Medpace Internship Program
For students wanting to gain professional experience and an introduction to the clinical research industry, an internship with Medpace offers the opportunity to explore career paths and develop valuable workplace skills.
Expand Your Professional Network
Our interns learn from the best in the business – Expanding their networks to Executive leadership who are doing groundbreaking work with Medpace. Students also have the opportunity to connect with others that share likeminded ideas and career goals.
Put Your Education to Work
Medpace offers internship opportunities for all degree types. Whether you are a life science, business, or IT student, our internships will allow you to utilize the skills you’ve learned in the classroom and apply them to practical, workplace situations.
Experience a Dynamic Workplace Culture
Interns can expect a culture of teamwork and collaboration in Medpace’s offices. This environment allows students to improve their time management, communication, and leadership skills.
The Details
Applicants have rights under Federal Employment Laws. Medpace participates in E-Verify.
About Medpace
We’ve built a unique culture where employees are part of a bigger purpose: to make a difference in the lives of millions today, tomorrow, and for years to come. Together, we improve lives.
Life at Medpace
People. Purpose. Passion. More than a slogan, it’s a philosophy that defines how we bring value to our clients and to one another. Every day.