Latest CSL Jobs

Associate Director, R&D Project Management

Leads the operational delivery of high-impact, global R&D projects within a cross-functional biotech environment. Focuses on strategic planning, budget and timeline management, risk mitigation, and stakeholder reporting. Provides mentorship to junior project management staff and ensures robust project execution across drug research, development, and manufacturing.

CSL

Hybrid Permanent

Associate Director, Clinical Trial Disclosure & Transparency

This role leads global clinical trial disclosure and transparency strategy, ensuring compliance with international regulations such as FDAAA 801, EU CTR, and MHRA requirements. The individual oversees study registration, results reporting, and layperson summaries, while managing redaction of confidential information for public release. They act as a key liaison with regulatory bodies and internal teams, driving process efficiency and vendor performance across the clinical development lifecycle.

CSL

Global Safety Lead - Formulation Safety

Leads global safety strategy for formulation safety within CSL's GSPV department, overseeing clinical safety evaluation across product lifecycles. Responsible for signal detection, risk management planning, and regulatory compliance across clinical development and post-marketing phases. Serves as safety representative in cross-functional teams, ensuring alignment with medical, regulatory, and business objectives.

CSL

Head, PV and Regulatory QA

This role leads the global quality and compliance function for pharmacovigilance (PV) systems, ensuring adherence to international regulations and internal standards across clinical safety, regulatory affairs, and medical affairs. The position combines strategic oversight with hands-on operational leadership, including audit strategy, inspection readiness, deviation and CAPA management, and cross-functional GxP guidance. It requires deep technical expertise in PV processes and strong leadership to drive quality across global teams and third-party vendors.

CSL

Specialist, R&D Contracts & Business Operations

This role supports R&D contract management and business operations within a global biopharmaceutical organization. The specialist will handle end-to-end contract processes including drafting agreements, managing purchase orders, ensuring compliance, and maintaining accurate records. Collaboration with cross-functional teams is essential to track obligations, ensure timely approvals, and promote operational efficiency in a hybrid working environment.

CSL

Hybrid Permanent

Head, PV and Regulatory QA

Leads global pharmacovigilance and regulatory quality assurance, ensuring compliance with GVP, ICH, and regulatory standards across clinical safety, medical affairs, and regulatory affairs. Designs audit strategies, manages inspections, and oversees deviation management, CAPA, and change control systems. Provides cross-functional GxP expertise and drives continuous improvement in PV quality systems.

CSL