Associate, Study Management III

• Supporting the Study Project Manager in strategic leadership of the cross-functional team through stakeholder engagement and influence to drive deliverables and timelines including study-level oversight and leadership of assigned activities within one or more global trials in a cross-functional environment for activities from inception through closure. • Vendor management, from initiation through closure, including deliverable oversight, and risk management for one or more vendors. • Recruitment management, from country feasibility through subject recruitment and retention. • Leadership of assigned meetings and training (internal and external) and provision of regular updates on study status, e.g., agenda and minutes. • Ensure inspection readiness and participate in related activities. • Risk identification, mitigation, and management. • Co-development and management of study materials and systems throughout study life cycle (e.g., Protocols, informed consent, clinical study report, training materials, newsletters, presentations, IP, CTMS, eTMF, EDC, IRT, ePRO, access management, etc.) • Provide engaging training to identified stakeholders as needed. • Support process improvement initiatives.