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Medpace is seeking a full-time, office-based Project Coordinator to join our Clinical Trial Management team in Denver. You will engage in day-to-day trial management, support the CTM, and coordinate meetings while maintaining accurate status reports and regulatory filing oversight.
Qualifications include a health/life sciences degree and prior pharmaceutical experience, plus strong Excel, organizational, and communication skills.
Medpace is seeking a full-time, office-based Project Coordinator to join our Clinical Trial Management team in Denver. You will engage in day-to-day trial management, support the CTM, and coordinate meetings while maintaining accurate status reports and regulatory filing oversight.
Qualifications include a health/life sciences degree and prior pharmaceutical experience, plus strong Excel, organizational, and communication skills.