Associate Clinical Project Manager

Job Title: Associate Clinical Project ManagerDepartment: Clinical Operations / Global Clinical SciencesOverview:Seeking an Associate Clinical Project Manager (ACPM) to support the successful execution of global clinical trials from protocol through study closeout.Key Responsibilities:Study & Documentation ManagementMaintain Trial Master File (TMF) in an inspection-ready stateSupport development and review of study documents (protocols, ICFs, CSRs, study plans)Assist with clinical data review to ensure quality and completenessSupport contract, budget, and invoice tracking activitiesProject Coordination & CommunicationCoordinate communication across internal teams, vendors, and CROsTrack study timelines, metrics, and status updatesSupport and document study team meetings and action itemsAssist with vendor and site coordinationQuality & ComplianceSupport audit and inspection readiness activitiesAssist with issue resolution and quality improvement initiativesEnsure compliance with GCP and regulatory requirementsTraining & Systems SupportAssist with development and tracking of study-specific trainingSupport investigator meetings and study start-up activitiesProvide support for CTMS and other clinical systemsQualifications:Bachelor’s degree required1–2 years of CRA or clinical research experienceUnderstanding of clinical trial phases (Phase I–IV)Strong organizational, communication, and problem-solving skills