Site Activation Manager I/II

Site Activation Manager I/II responsible for overseeing end-to-end site start-up activities for clinical trials, collaborating with Business Development, Alliance Management, Contracts and Proposals Development, SSU Country Managers, Project Management, Clinical, Data Management, and Medical Writing. Identifies regulatory pathways for site start-up, ensures on-time delivery of all SSU deliverables from site identification through activation and lifecycle maintenance, and maintains high-quality standards aligned with contracted deliverables. Builds and maintains customer relationships, tracks integrated start-up timelines, prepares weekly progress reports, and manages budgets to ensure project profitability. Develops SSU strategies, conducts Regulatory Impact Assessments for amendments, supports SIS/ICF development with medical, and coordinates country-specific submissions. Contributes to change initiatives within SSU and presents outcomes at client meetings, while leveraging tools for scope, timeline, and resource management. This posting is intended for a possible upcoming opportunity rather than a live role and may be added to a talent pipeline.