Teams at Nuvation Bio

Lead and manage clinical trial operations including CRO and vendor oversight, study planning, budgets, site selection, regulatory compliance (GCP/ICH), document development, inspection readiness, and cross-functional coordination for oncology trials across phases.

Lead analytical development and QC activities from early development through commercial support, including method development/validation/transfer, stability and release testing, vendor/CRO/CMO management, regulatory submission authorship, audits/inspections, and MAH oversight for China market with routine on-site supervision.

Lead commercial sales for an assigned oncology territory, build relationships with HCPs and KOLs, generate demand, execute account plans, leverage data and omnichannel tools, support product launches, represent company at conferences, and comply with regulatory and credentialing requirements.