Jobs at Syndax Pharmaceuticals

Leads domestic and international pharmaceutical logistics, including transportation, warehousing, distribution, customs, 3PLs, serialization, and cold-chain operations. Ensures GDP, GMP, DSCSA, quality, traceability, and compliance requirements. Manages logistics performance, risk mitigation, costs, deviations, CAPAs, temperature excursions, and business continuity while partnering with internal teams and external providers.

Leads enterprise commercial strategy and long-range account planning for complex academic and integrated health systems. Drives formulary access, pathway adoption, standardized product use, institutional education, and cross-functional execution across oncology accounts. Influences healthcare leadership and C-suite stakeholders while supporting account managers and coordinating market access, clinical education, and system-of-care partners. Requires frequent overnight travel and occasional weekend travel.

Leads global supply chain network planning and risk management across clinical and commercial pharmaceutical programs. Oversees S&OP, demand and supply planning, inventory and capacity strategy, production control, scenario planning, business continuity, and supply risk mitigation. Partners across manufacturing, logistics, quality, regulatory, finance, and commercial functions to ensure reliable patient supply. Builds planning processes, systems, analytics, governance, and a high-performing global team while supporting launches, market expansion, and lifecycle changes.

Lead market access strategy and execution for Syndax’s hematology-oncology portfolio, including payer strategy, reimbursement, pricing, contracting, patient services, trade and distribution. Partner with Commercial, Medical Affairs, Finance, Legal, Regulatory, and Clinical Development to support evidence generation, product launches, lifecycle management, and international expansion. Build and lead a high-performing market access organization while managing payer relationships, healthcare policy implications, and long-term patient access and franchise growth.

Provides biostatistical leadership for clinical trial design, analysis, regulatory submissions, and evidence generation. Oversees CRO deliverables, statistical quality control, analysis plans, protocols, clinical study reports, and regulatory interactions. Collaborates cross-functionally with clinical, medical affairs, and other teams while leading biostatistics initiatives and process improvements. Requires advanced clinical trial expertise, regulatory knowledge, leadership, communication skills, and SAS programming ability.

Leads end-to-end bioanalytical strategy for small-molecule and biologic development programs across nonclinical and clinical portfolios. Oversees assay development, validation, sample analysis, CRO selection and performance, regulatory documentation, and cross-functional collaboration. Serves as the bioanalysis subject matter expert and supports regulatory interactions and due diligence. At the Senior Director level, provides organizational leadership, mentors scientists, manages resources and budgets, and develops the function’s long-term capabilities.

Leads supplier quality management for GxP service providers, suppliers, contract laboratories, distribution partners, and outsourced vendors. Responsibilities include risk-based supplier qualification, audits, lifecycle oversight, quality metrics, quality technical agreements, corrective actions, inspection readiness, and regulatory compliance. The role collaborates with Quality, Supply Chain, Regulatory, Clinical Operations, Pharmacovigilance, IT, and external partners while supporting supply chain expansion, vendor transitions, and continuous improvement.

Provides expert statistical programming support for clinical trials and drug programs using SAS. Produces and validates tables, listings, figures, CRF tabulations, pooled analyses, biomarker and HEOR analyses, and regulatory responses. Collaborates with biostatisticians, data managers, vendors, and cross-functional teams while ensuring compliance with statistical analysis plans, CDISC standards, FDA regulations, ICH guidelines, and applicable regulatory requirements.

Oversee GMP quality activities for investigational drug substances, drug products, and clinical finished goods manufactured by external partners. Review batch, testing, packaging, labeling, and release documentation; manage deviations, investigations, CAPAs, change controls, complaints, and OOS/OOT events. Partner cross-functionally to mitigate compliance and patient-safety risks, support clinical supply continuity, author quality documents, and ensure regulatory and company quality-system compliance.