CSL
Jobs at CSL
Let Your Resume Do The Work
Upload your resume to be matched with jobs you're a great fit for.
Success! We'll use this to further personalize your experience.
Recently posted jobs
Biotech
Leads global and site security programs across facilities, offices, and laboratories. Responsibilities include security operations, risk and vulnerability assessments, crisis response, investigations, threat awareness training, vendor and contract coordination, governance, technology roadmaps, reporting, and continuous improvement. The role manages security budgets, supports law-enforcement relationships, advises executive leadership, and maintains 24/7 readiness for security incidents and emergencies.
Biotech
Leads immunology clinical research from target prioritization and preclinical translation through first-in-disease programs. Partners with discovery, translational medicine, clinical development, and business development teams to evaluate assets, shape clinical strategies, design early-phase studies, define biomarkers and patient populations, and support go/no-go decisions. Serves as a hands-on clinical subject matter expert in autoimmune and inflammatory diseases, representing the organization with scientific leaders, investigators, regulators, and internal stakeholders.
Biotech
Lead statistical strategy and execution for clinical development programs. Oversee study design, SAP authoring, data analysis, TFL/CDISC deliverables, CRO/vendor oversight, regulatory interactions, and interpretation of results to support submissions and program decisions.
Biotech
Leads project management for biotech due diligence and external innovation activities, including in-licensing and partnership evaluations. Develops integrated plans, timelines, budgets, risk tracking, governance tools, dashboards, and decision-support materials. Coordinates scientific, clinical, regulatory, legal, IP, commercial, and finance stakeholders; ensures timely, compliant evaluations; supports senior leadership decisions; and improves due diligence workflows and tools. The role also mentors junior team members and manages relationships with external partners.
Biotech
Lead epidemiology strategy and programs for assigned products, design and execute studies, manage data and vendors, contribute to regulatory submissions, drive RWE use, perform benefit-risk assessments, and support departmental process improvement and cross-functional leadership.
Biotech
Provides strategic and hands-on biostatistical leadership across pharmaceutical discovery, translational, biomarker, and early research programs. Designs studies, analyzes complex biological datasets, develops advanced statistical methods and reproducible R workflows, and translates evidence into portfolio decisions. The role collaborates with quantitative and scientific functions, supports publications and external partnerships, mentors statisticians, and advances data-driven analytical practices.
Biotech
Drafts, reviews, and negotiates commercial agreements throughout the contracting lifecycle. Maintains contract templates, FAQs, and CLM records; advises business partners on legal matters; delivers training; and identifies opportunities to improve legal service efficiency through process optimization, automation, legal design, and technology. The role collaborates across departments and may require occasional domestic or international travel.
Biotech
Leads CSL Behring’s state government affairs strategy across the Southeast US. Builds relationships with legislators, regulators, patient advocates, trade associations, and consultants; analyzes legislation and policy; advocates for Medicaid access and plasma donation; develops coalitions and action plans; represents company operations; and communicates policy insights to leadership and cross-functional teams.
Biotech
Lead people-analytics strategy for Talent Acquisition and Talent Development. Drive end-to-end analysis of complex workforce problems, deliver evidence-based recommendations to senior leaders, ensure data governance and quality, coach junior analysts, build metrics frameworks, and conduct benchmarking and external research to inform workforce strategy.
Biotech
Lead governance, review, and validation of clinical data deliverables ensuring CDISC/SDTM compliance and submission readiness. Oversee EDC/eCRF design, data quality control frameworks, vendor deliverable review, reporting/visualization, and integration of external data sources. Support scalable data platforms, automation, and AI-enabled capabilities while partnering with Data Management, Statistics, and vendors to ensure data traceability and regulatory alignment.
Biotech
Lead global IT sourcing strategy and a multi-year technology modernization agenda. Manage $450M spend, strategic supplier relationships, governance, risk, and value delivery. Oversee category management (cloud, software, infrastructure, cyber), negotiations with hyperscalers and SaaS vendors, stakeholder engagement, and build a high-performing sourcing organization.
Biotech
Lead global vaccines safety science activities including pharmacovigilance governance, regulatory compliance, signal detection, safety data analysis, inspection readiness, PSMF maintenance, process optimization, and technical translation of business requirements into reporting and visualization solutions. Manage teams, contribute to post-marketing and study safety reporting, and support regulatory submissions and audits.
Biotech
Leads global technology sourcing strategies across software, SaaS, cloud, infrastructure, hardware, telecommunications, cybersecurity, and related services. Manages high-value competitive sourcing, negotiations, contracts, supplier relationships, risk mitigation, stakeholder alignment, and procurement transformation. Analyzes spend and market trends to deliver savings and value while ensuring governance, compliance, continuity, and supplier performance. Provides strategic guidance to sourcing managers and engages senior leaders and global technology suppliers.
Biotech
Leads CSL’s global knowledge management and insight advisory service, overseeing strategy, governance, budgets, personnel, vendors, systems, data standards, and information resources. The role advances AI-focused digital innovation, manages research databases and APIs, supports scientific and regulatory information access, develops performance metrics, and leads global teams through coaching and collaboration. It requires extensive pharmaceutical, knowledge management, data governance, vendor management, and people leadership experience.
Biotech
Leads technology platform strategy, delivery coordination, operational planning, complex projects, service improvements, and adoption initiatives. Partners with business, IT, architecture, vendors, and global stakeholders to maintain secure, compliant, scalable, and reliable platforms. Oversees roadmaps, governance, performance, risk, regulatory compliance, SDLC adherence, validation, data governance, and audit readiness while translating business needs into sustainable technology solutions.
Biotech
Lead development and coordination of global regulatory CMC strategies for CAPEX, compliance, and outsourcing. Support digital innovation (including AI/ML), manage vendor relationships, monitor global regulations, advise senior leadership on regulatory implications, and implement regulatory policies, SOPs, and KPIs to drive operational alignment across Global Regulatory Affairs, R&D, Quality, and Global Operations.
Biotech
Provide legal counsel and contract drafting/negotiation for global clinical development, advise on regulatory issues (GCP/ICH, FDA), escalate complex matters, create templates, deliver training, and support cross-functional global projects.
Biotech
Lead regional enterprise contracting for the Americas, build stakeholder and external partner relationships, lead negotiations, improve contracting processes, manage risk and compliance, and drive legal technology and continuous improvement initiatives.
Biotech
Lead regional regulatory strategy and health authority interactions for assigned products, support preparation of regulatory submissions and Module 1 documentation, contribute to global regulatory strategy (GRAST), maintain regional regulatory knowledge and stakeholder communications, update regulatory systems (e.g., Veeva), and drive timely, positive regulatory outcomes in a hybrid US location.
Biotech
The Associate Director, Federal Government Affairs will manage strategies for CSL Behring's federal interests, engage with stakeholders, provide policy insights, and collaborate on advocacy efforts.
