Director, Global Study Start-Up & Regulatory Submissions
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Management
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Research/Development
Job Description & How to Apply Below
Medpace, a full-service CRO, seeks an office-based Director of Study Start-Up to lead our Study Start-Up/Regulatory Submissions team in Cincinnati. The role requires CRO experience and strong leadership to align start-up activities with clinical operations and regulatory timelines.
You will oversee process improvements, mentor a growing team, and develop client relationships while contributing to global study start-up initiatives.
Step into the Director, Global Study Start-Up & Regulatory Submissions role at Medpace in Cincinnati, OH, United States and grow with us.
Our organisation is growing, and we are hiring a Director, Global Study Start-Up & Regulatory Submissions in Cincinnati, OH, United States.
This opportunity is for the Director, Global Study Start-Up & Regulatory Submissions role at Medpace.
We are seeking a motivated Director, Global Study Start-Up & Regulatory Submissions to join Medpace in Cincinnati, OH, United States.
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