Teams at Tango Therapeutics

Leads clinical technology systems across study startup, data generation, integrations, testing, support, decommissioning, and archival. Serves as subject matter expert for eCOA, IRT, and centralized imaging, ensuring data integrity, regulatory compliance, issue resolution, and inspection readiness. Partners with Clinical Data Management, Clinical Operations, Biostatistics, and other stakeholders on requirements, implementation, documentation, KPIs, UAT, system integrations, and clinical data quality.

Leads GCP and GLP quality assurance across clinical and nonclinical programs. Responsibilities include risk-based audits, CRO and vendor oversight, inspection readiness, quality-event investigations, root-cause analysis, CAPA development, quality agreements, SOPs, training, and regulatory inspection responses. The role provides strategic QA guidance to Clinical Operations, clinical trial teams, nonclinical groups, and external partners while ensuring compliance with global regulations and FDA BIMO requirements.

Leads pharmacovigilance and drug safety activities across clinical development and commercialization. Responsibilities include signal detection, literature reviews, benefit-risk assessments, safety governance, aggregate safety report authorship, clinical document review, risk management, regulatory compliance, audits, inspections, and collaboration with cross-functional and partner teams.