"Business rationale Sustain critical post marketing RWE analytics that support Medical evidence generation and external scientific communication (e.g., evidence generation, insight translation, publications). Maintain specialized capabilities (clinical trial data OR OMOP CDM/real world data) to meet timelines and ensure compliant, high quality outputs and scientific collaboration/support. Mitigate capacity risk for ongoing and upcoming studies and avoid delays that impact HCP-facing scientific responsiveness and internal decision support."

"1) Master’s degree or above 2) Major in Statistics, Epidemiology, or related discipline 3) Either (a) experience with phase 2–3 clinical trials and adaptive design, OR (b) experience with OMOP CDM and real world studies 4) Good knowledge and skill of R coding and sample size determination 5) Industry experience preferred 6) Strong interest in Medical Affairs evidence generation activity and process management (post marketing study focus) 7) English reading and writing proficiency 8) Preferred location is Beijing "