Jobs at IDEAYA Biosciences

Leads IDEAYA’s integrated investor relations and corporate communications function, advising the CEO, CFO, executive team, and Board. Responsibilities include investor engagement, earnings materials, corporate narrative, executive messaging, media relations, internal communications, reputation and crisis communications, disclosure compliance, and milestone communications. The executive will build the function from the ground up, hire and develop a team, manage external partners, and support the company’s transition from clinical-stage to commercial-stage biotechnology operations.

Lead global supply chain operations across clinical and commercial products, including demand and supply planning, procurement, logistics, inventory optimization, ERP management, and risk mitigation. Drive S&OP, maintain lot and batch traceability, ensure cGMP and regulatory compliance, manage cold-chain logistics, and use analytics to improve forecasting and operational performance. Collaborate with Clinical, Commercial, Manufacturing, Quality, Regulatory, Finance, and IT stakeholders while leading cross-functional improvement initiatives.

Supports the Chief Commercial Officer through complex calendar and travel management, meeting preparation, confidential communications, leadership coordination, and stakeholder engagement. Also manages Commercial operations, including planning, budgets, vendors, project timelines, dashboards, action tracking, process improvements, and event logistics. Partners cross-functionally with Medical Affairs, Clinical Development, Finance, Legal, HR, Procurement, and Investor Relations in a fast-paced biotech environment.

Oversee monitoring quality across multiple oncology clinical trials, including CRO monitoring activities, oversight plans, monitoring reports, risk assessments, corrective actions, SOPs, audits, and inspections. Partner with clinical operations teams and CROs to ensure GCP, regulatory, protocol, and data-quality compliance. Lead training, metrics tracking, process improvements, and senior-management reporting. The role is onsite four days per week in South San Francisco or San Diego and requires up to 80% travel.

Leads commercial supply strategy and launch readiness for a pharmaceutical product. Responsibilities include demand and supply planning, production scheduling, S&OP, inventory management, external manufacturing and vendor governance, packaging and serialization readiness, logistics, cold-chain controls, KPI reporting, regulatory and quality coordination, and financial forecasting. The role requires cross-functional leadership, strong pharma supply chain expertise, and the ability to build processes in a fast-paced environment.

Leads safety biostatistics and biometrics strategy for oncology drug development, overseeing clinical trial design, protocols, statistical analysis plans, safety analyses, regulatory submissions, and publications. Manages internal and external biostatistics teams, mentors development staff, ensures statistical quality, and supports Drug Safety and Pharmacovigilance activities. Represents the biostatistics function with regulatory agencies, vendors, key opinion leaders, and cross-functional stakeholders.

Leads SEC filings, technical accounting, financial disclosures, SOX compliance, equity accounting, audit coordination, and reporting process improvements. Prepares 10-K and 10-Q filings, evaluates complex transactions under U.S. GAAP, monitors regulatory changes, supports Audit Committee materials, and partners with auditors and cross-functional teams. Provides project leadership and coaching while improving controls, data quality, and scalable accounting operations.

Lead strategic and operational project management for IDE892, a complex oncology development program. Responsibilities include owning the integrated development plan, timeline, budget, milestones, risks, cross-functional meetings, regulatory readiness, clinical study execution, scenario planning, and senior leadership reporting. The role also manages Roche collaboration governance and external partners while aligning scientific, clinical, regulatory, commercial, and portfolio priorities.

Leads the launch and adoption of darovasertib across California and Nevada. Develops sophisticated oncology account and territory strategies, builds relationships with academic and community healthcare stakeholders, activates referral networks, translates clinical data into compliant product education, supports patient access, and partners cross-functionally with Medical Affairs, Value & Access, and Patient Services. Uses analytics to prioritize accounts and resources while managing CRM reporting, budgets, compliance, and approximately 80% travel.

Leads oncology product launch and adoption across California and Nevada. Develops territory and account strategies, builds relationships with academic and community oncology stakeholders, activates referral networks, translates clinical data into compliant education, and collaborates with Medical Affairs, Value & Access, and Patient Services. Manages complex accounts, reimbursement and fulfillment pathways, analytics, budgets, CRM reporting, and regulatory compliance. Requires extensive pharmaceutical and oncology sales experience, with approximately 80% travel.