Key Responsibilities:Partner with Business Development to support feasibility assessments and site qualification activitiesCollaborate with regulatory teams to ensure accurate and complete feasibility documentationBuild strong sponsor relationships by understanding client needs and ensuring confidence in study executionContribute to proposal development, including cost estimation and preparation of sponsor-ready submissionsLead project kick-off meetings and align cross-functional teams and external stakeholdersCoordinate with vendors and consultants to define scope, timelines, and deliverablesDevelop and manage project timelines, proactively identifying risks and implementing mitigation strategiesServe as the primary point of contact for sponsors, ensuring clear communication and on-time deliveryMonitor project progress, budgets, and performance metrics; analyze trends and address issues proactivelyReview financials, approve vendor expenses, and partner with Project Finance on scope and budget changesEnsure high-quality study closeout deliverables, respond to sponsor inquiries, and lead lessons learned for continuous improvementWhat We're looking for Clinical Project Manager:CPM: Associates / equivalency (60 or more college credit hours) in related field + 2 years as a Project Manager; OR Bachelor of Science in related field + 1 year as a Project Manager. Job Overview:The Clinical Project Manager (CPM) is the single, accountable leader for early-phase (FIH, SAD/MAD, food-effect, DDI, 14C etc.) clinical trials, translating Sponsor protocols into integrated project plans and guiding cross-functional teams from study initiation and first-subject-in through CSR submission and TMF delivery.