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The Associate Director will manage financial planning for Clinical Operations, budgeting, forecasting, and detailed reporting to support strategic decisions.

This role leads Global Quality Assurance activities for pharmacovigilance, ensuring compliance with regulations and standards through oversight, audits, and risk mitigation strategies.

The VP will lead the global development strategy for orelabrutinib, ensuring efficient execution of Phase 3 programs, risk management, and strategic communications with leadership and stakeholders.

The Director of Pharmacovigilance will oversee clinical trial PV support, manage safety data, develop reports, and ensure compliance with regulations while working in a collaborative environment.

The Program Manager leads and executes programs in pharmaceutical development, ensuring alignment with business goals and managing cross-functional activities to deliver desired outcomes.

The Director of DMPK will lead drug metabolism and pharmacokinetics functions, executing DMPK strategies across all development stages, managing CROs, and collaborating with cross-functional teams on regulatory submissions.

The VP will oversee small molecule drug development and manufacturing strategies, manage CDMO relationships, ensure regulatory compliance, and build a talented team.

Lead the market access strategy and execution for Zenas BioPharma, ensuring optimal patient access across all payer types while managing a high-performing team and collaborating with cross-functional partners.