A company is looking for a Senior Clinical Data Associate - Risk-Based Quality Monitoring (RBQM).Key ResponsibilitiesOversee RBQM-related data management activities for assigned projectsManage and collaborate with CROs to ensure study deliverables and timelines are metGenerate and review study documents and ensure clinical data quality meets regulatory standardsRequired QualificationsB.
S. / B.A. in a science or technical discipline with 6 years of clinical data management experience, or M.S. / Ph.D. / M.D.
with 4 years of experienceFamiliarity with clinical trial life cycle and data management for Phase I-IV trialsPrior experience with RBQM methodologies and TSDV managementWorking knowledge of ICH / GCP and regulatory requirementsExperience managing CRO vendors
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