.Company DescriptionJob DescriptionSMA IIIAs a Clinical Trial Manager, you will be part of a dynamic, centralized study management team that is responsible for the execution of our global clinical trials and a key member of the study team. The Clinical Trial Manager works as an independent, contributing member of a cross-functional and global partnership to plan, execute and manage one or more Phase 0-4 clinical trials under the guidance of the Study Project Manager and SMA Manager. The Clinical Trial Manager works to ensure that assigned studies are executed with quality and efficiency, in accordance with timelines and budget to support broader company strategic objectives.Primary ResponsibilitiesStudy-level oversight and leadership of one or more global trials in a cross-functional environment for activities from inception through closure, connecting functional work and strategic work across the global study, including but not limited to:Supports the Study Project Manager in strategic leadership of the cross-functional team through stakeholder engagement and influence to drive deliverables and timelines, including strategy development, meeting facilitation, and timely documentation at the study level to drive for timely execution of clinical trial(s).Vendor management, including Request for Proposal (RFP)/initiation, selection, Scope of Work development & review, deliverable oversight, and risk management for one or more external vendors, e.G., central lab, recruitment, imaging, internal and external committees.Leadership of assigned meetings (cross-functional (internal), vendor, and/or investigator) and provision of regular updates on study status, e.G., agenda development, minutes curation and filing.Ensure inspection readiness and participate in related activities.Risk identification, mitigation, and management, including timely issue review, escalation, and management to support trend analysis and risk prevention.Co-development and management (review, revision, tracking and filing) of study materials, including but not limited to: protocols, regulatory submissions, patient reported outcome measures, study execution plan, informed consent, site budgets and agreements, clinical study report, training materials, newsletters, presentations for various stakeholders.CTMS and eTMF management to ensure compliance/inspection readiness, support trend analyses and support timelines.EDC, IRT, and ePRO, which includes review of design specifications, participation in user acceptance testing, and contribution to development and review of associated plans and key risk indicators, as well as system management activities like access support, query resolution, and oversight.Management of investigational product and other associated study supplies.Provide engaging training to identified stakeholders as needed, e.G., study team members, vendors.Support global submission strategies.QualificationsBachelor's Degree or OUS equivalent required
