Teams at Kymera Therapeutics

Directs clinical data management activities across multiple studies, overseeing CRO deliverables, data collection tools, user acceptance testing, data quality control, cleaning, query resolution, medical coding, timelines, and budgets. Manages vendors and mentors internal team members while ensuring data integrity and security. Contributes to SOPs, process improvements, technology selection, and best practices. Requires extensive biotechnology or pharmaceutical clinical data management experience and expertise in CDISC and medical terminology standards.

Leads statistical strategy for clinical studies and programs, contributing to development plans, regulatory submissions, protocols, statistical analysis plans, clinical study reports, publications, and presentations. Oversees statistical programmers and CROs, ensures regulatory compliance and output quality, supports CRF design, and may manage direct reports. Collaborates with cross-functional teams and communicates statistical findings to non-statisticians.

The Director, Trial Master File will lead TMF platform implementation, oversee compliance, standardize processes, and ensure inspection readiness across clinical operations.