• Contribute to the implementation of the overall clinical program management strategy in collaboration with the Sr. Director, Clinical Program Management and functional leaders • Support clinical program management activities across Adverum, working with key functional representatives to understand study status, identify risks, and escalate issues as appropriate • Plan, align, communicate, and coordinate detailed and high‑level cross‑functional Phase 3 study timelines • Collaborate with cross‑functional teams to ensure alignment with integrated Phase 3 timelines and overall program milestones • Facilitate resolution of timeline and resource discussions, balancing team capacity with study objectives and delivery expectations • Track Phase 3 start‑up and operational activities to ensure timelines remain on track; proactively identify risks and support escalation with recommended mitigation strategies • Drive coordination across teams to ensure timely planning, sequencing, communication, and completion of interdependent activities • Maintain critical path visibility to key study and program milestones, ensuring deliverables are clearly defined and achieved • Apply best practices for clinical trial conduct across all aspects of study execution, partnering with Clinical QA as needed • Assess and communicate the impact of changes to Phase 3 study design or program strategy • Support cross‑functional forums to monitor trial progress, risks, action items, and timeline dependencies • Collaborate regularly with cross‑functional PMO partners to ensure alignment with non‑clinical planning and deliverables