Leads strategic sourcing and evaluation of early-stage innovation in haematology, from preclinical to Phase 1 assets. Drives due diligence, shapes partnering strategies, and executes transactions in collaboration with Business Development. Embedded in the Therapeutic Area Leadership Team to influence portfolio planning and external innovation priorities.
The Associate Director, Biostatistics, leads statistical contributions to clinical development programs, including study design, data analysis, and regulatory submissions. They collaborate with cross-functional teams, manage outsourcing, and ensure the quality and timeliness of deliverables.
This role involves designing and executing experiments to develop next-generation platforms for continuous evolution, focusing on engineering orthogonal replication systems that enable rapid gene evolution while maintaining host viability. The researcher will analyze complex datasets using computational tools, contribute to novel methodologies, and collaborate across multidisciplinary teams to advance fundamental and applied research in generative biology. Emphasis is placed on innovation in evolutionary systems, mentoring junior scientists, and translating discoveries into real-world applications in health and sustainability.
The Controlled Environment Lead will build and oversee plant growth and phenotyping facilities, ensuring controlled and reproducible environments for high-impact plant science research. Responsibilities include hands-on cultivation, data collection, and leading the team to support scientific and commercial goals.
This role leads the statistical strategy for clinical development programs, overseeing study design, data analysis, and regulatory submissions. The individual will guide biostatistical input across trials, interact with regulatory authorities, and ensure accurate reporting of results. Collaboration with cross-functional teams and oversight of internal or outsourced programming efforts are key aspects of the position.
Leads global safety strategy for formulation safety across the product lifecycle, focusing on clinical safety evaluation, signal detection, and risk management. Oversees production of key pharmacovigilance documents and ensures compliance with regulatory standards. Acts as safety representative in cross-functional teams and drives safety specifications and risk mitigation plans.
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.
The Quality Manager role involves maintaining and improving quality management systems, ensuring compliance with regulatory requirements, and supporting inspection readiness across CSL's global affiliates. You will collaborate with cross-functional teams, manage quality processes, and implement electronic quality systems.
The Quality Manager role involves maintaining and improving CSL's quality management systems across Europe and global affiliates. Responsibilities include inspection readiness, process harmonization, and supporting quality initiatives. The role requires collaboration with multiple functions and stakeholders, with a focus on compliance and continuous improvement.
The Quality Manager role involves maintaining and improving CSL's quality management systems across Europe and global affiliates. Responsibilities include coordinating inspection readiness, supporting compliance activities, and implementing global quality initiatives. The role requires strong knowledge of pharmaceutical regulations and quality systems, with a focus on collaboration and process improvement.
This role involves managing and maintaining quality processes, ensuring compliance with regulatory requirements, and supporting inspection readiness across CSL's global affiliates. You will collaborate with cross-functional teams to implement quality initiatives and improve systems.
This role involves managing and improving quality systems across CSL's European affiliates, ensuring compliance with regulatory requirements. Responsibilities include coordinating inspection readiness, maintaining quality KPIs, and supporting global quality initiatives. The position requires strong knowledge of pharmaceutical regulations and quality systems, with a focus on continuous improvement and cross-functional collaboration.
The Quality Manager role involves maintaining and improving CSL's Affiliate Quality Management System across Europe and global affiliates. Responsibilities include inspection readiness, quality system governance, process harmonization, and supporting global quality initiatives. The role requires collaboration with multiple functions and stakeholders, including Quality, Regulatory Affairs, and Commercial Operations.
The Quality Manager role involves maintaining and improving CSL's quality management systems across Europe and global affiliates. Responsibilities include inspection readiness, process harmonization, and supporting quality initiatives. The role requires strong knowledge of pharmaceutical regulations and quality systems, with a focus on collaboration and continuous improvement.
This role involves managing and improving quality systems across CSL's European and global affiliates, ensuring compliance with regulatory requirements and CSL standards. Responsibilities include coordinating inspection readiness, maintaining quality KPIs, and supporting global quality initiatives.
