Clinical Trials Project Specialist - Study Ops & Tracking
PPG US ProPharma Group, LLC
ProPharma is seeking a Clinical Project Specialist to provide administrative and project management support for assigned clinical studies, coordinating with study teams to ensure compliant and timely execution. The role involves document development, tracking, site materials, and study trackers using CTMS, eTMF, and other systems, with strong emphasis on communication and organization. Candidates should have a bachelor’s degree and 2+ years in pharma/biotech CRO settings, with experience in #J-18808-Ljbffr PPG US ProPharma Group, LLC
Vacancy posted 2 days ago
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