Senior Associate, Programmes at Evidence Action

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• Coordinate targeted treatment, surveillance, classification, and related programme workstreams in line with national STH/SCH guidance. • Provide day-to-day technical assistance to government counterparts and support planning, coordination, stakeholder engagement, advocacy, and partner meetings. • Review programme plans, guidelines, SOPs, and reports; document implementation challenges, lessons, and recommendations. • Maintain and update county/IU classification and surveillance data, support impact assessments and field surveillance, and facilitate timely notify–verify–investigate–respond actions. • Ensure accurate flow of classification, surveillance, coverage, and treatment data into KHIS, eCHIS, IDB, and other reporting systems. • Support JAP/JRSM submissions, drug quantification, delivery monitoring, redistribution, and supply-chain reporting in collaboration with MoH and KEMSA. • Coordinate county advocacy, training cascades, community mobilization, MDA scheduling, field supervision, and implementation monitoring. • Ensure MDA occurs only where indicated, monitor coverage, dosing, compliance, adverse events, and implementation fidelity, and escalate critical issues promptly. • Train and supervise data collectors and field teams, maintain accurate programme records, and support post-MDA reconciliation and reporting. • Support evidence and classification documentation for national reporting and validation processes, including EPHP requirements, and undertake other assigned duties. • Timely, complete, and accurate programme reports and government technical assistance. • Accurate and timely JAP/JRSM submissions aligned with current classification and treatment needs. • Timely drug delivery monitoring, redistribution, and resolution of supply issues. • Training and targeted MDA activities completed on schedule and according to guidance. • Same-day escalation of severe adverse events and confirmed surveillance signals.