Teams at Maplight Therapeutics

Support clinical operations across all trial phases: manage TMF and study documents, coordinate systems access, liaise with sites/CROs/vendors, prepare meeting materials and minutes, maintain trackers, assist with clinical trial insurance and data review, and ensure compliance with SOPs and ICH-GCP.

Lead statistical aspects of clinical projects: design sample size/power, author SAP and statistical protocol sections, oversee CRO statistical deliverables, contribute to CSR and regulatory documents, support publications, and collaborate with cross-functional clinical and regulatory teams.

Lead and standardize Clinical Program Management across the clinical development portfolio. Oversee program planning, execution, governance, risk mitigation, cross-functional alignment, and resource management. Develop the PM team, implement best practices and enterprise tools, and support decision-making to ensure consistent, high-quality execution from preclinical into clinical stages.