Career Opportunities for PhD Professionals

Featured Opportunities

Explore what it is really like to work at one of the top global leaders in the full-service CRO industry.

Medpace offers a variety of opportunities for PhDs to put their expertise in motion while performing an integral role in the research and development of drugs and medical devices; many opportunities do not require any previous experience. Although some of our opportunities require a PhD in Life Sciences, we encourage others to apply for a position that is better aligned in their respective area. Below are a few of our opportunities:

Clinical Trial Managers

Medpace is a scientifically led organization that provides full-service clinical development services to our Sponsors, giving the Medpace project teams the empowerment to truly lead and execute clinical trials. Medpace is currently looking for Clinical Trial Managers (CTMs) to lead clinical research studies.

Associate Clinical Trial Manager – Dallas, TX

The aCTM will be a part of the Clinical Trial Management team and support Project Coordinators and Clinical Trial Managers in performance of project management activities.

Associate Clinical Trial Manager – Denver, CO

The aCTM will be a part of the Clinical Trial Management team and support Project Coordinators and Clinical Trial Managers in performance of project management activities.

Clinical Research Associate – Cincinnati Entry Level

I have healthcare related experience and/or a Bachelor's, Master's, PharmD, or PhD in a life science field and am interested in transitioning to a CRA position through the Medpace PACE® Training Program.

Clinical Research Associate – Dallas Entry Level

Directors

Medpace clinical operations activities are growing rapidly, and we are currently seeking Directors to join our global Clinical Operations team in our Global Headquarters in our Cincinnati, OH office.

Other Opportunities

Entry Clinical Trials Feasibility Specialist

By working cross functionally with our clinical operations, medical and regulatory submissions teams, as well as through analyzing data from internal and public data sources, this individual will provide strategic insights on country selection and enrollment planning for global clinical trials.

Entry Informatics Analyst

Feasibility Informatics Analysts will work collaboratively with our clinical operations, medical and global feasibility teams to perform research as well as organization and analysis of data.

Clinical Data Coordinator

Our corporate activities are growing rapidly, and we are currently seeking a full-time, office-based Clinical Data Coordinator to join our Data Management team.