CSL Limited

Title: Associate Director, Federal Goverment Affairs Location: Americas, US-Washington DC Job Description: The Opportunity: Reporting to the Head of US Patient Advocacy & Government Affairs, as the Associate Director, Federal Government Affairs, you will support the development and execution of strategies to advance CSL Behring’s interests in federal legislative and regulatory matters. You will manage key projects and relationships with federal stakeholders, industry associations, and advocacy groups to influence policy outcomes that impact patient access and company priorities. You can be based out of our King of Prussia, PA corporate headquarters or our Washington, D.C. office. This is a hybrid role, which offers a combination of an onsite and remote work schedule. #LI-hybrid The Role: - Monitor and analyze federal legislative and regulatory developments affecting CSL Behring. - Execute engagement plans with federal government officials, trade associations, and advocacy organizations. - Provide policy insights and recommendations to internal stakeholders; prepare briefing materials and reports. - Collaborate with cross-functional teams (Market Access, Regulatory, Communications) to align advocacy strategies. - Represent CSL Behring in selected industry forums and working groups. - Draft policy communications, testimony, and position statements as needed. Your Skills & Abilities: - Bachelor’s degree required; advanced degree in law, public policy, or health-related field preferred. - 8–10 years of experience in healthcare government/public affairs or related field. - Strong understanding of federal legislative and regulatory processes. - Proven ability to manage complex projects and build relationships with policymakers and industry stakeholders. - Excellent communication and advocacy skills. - Strategic thinking and ability to influence policy outcomes. - Strong collaboration and stakeholder engagement skills. - Ability to synthesize complex policy issues into actionable insights. About CSL Behring CSL Behring is a global biotherapeutics leader driven by our promise to save lives. Focused on serving patients’ needs by using the latest technologies, we discover, develop and deliver innovative therapies for people living with conditions in the immunology, hematology, cardiovascular and metabolic, respiratory, and transplant therapeutic areas. We use three strategic scientific platforms of plasma fractionation, recombinant protein technology, and cell and gene therapy to support continued innovation and continually refine ways in which products can address unmet medical needs and help patients lead full lives. CSL Behring operates one of the world’s largest plasma collection networks, CSL Plasma. Our parent company, CSL, headquartered in Melbourne, Australia, employs 32,000 people, and delivers its lifesaving therapies to people in more than 100 countries. To learn more about CSL, CSL Behring, CSL Seqirus and CSL Vifor visit https://www.csl.com/ and CSL Plasma at https://www.cslplasma.com/. Our Benefits For more information on CSL benefits visit How CSL Supports Your Well-being | CSL. You Belong at CSL At CSL, Inclusion and Belonging is at the core of our mission and who we are. It fuels our innovation day in and day out. By celebrating our differences and creating a culture of curiosity and empathy, we are able to better understand and connect with our patients and donors, foster strong relationships with our stakeholders, and sustain a diverse workforce that will move our company and industry into the future. To learn more about inclusion and belonging visit https://www.csl.com/careers/inclusion-and-belonging

Title: Associate Director, US Patient Advocacy Location: Americas, US-PA, King of Prussia, CSL Behring Job Description: The Opportunity: Reporting to the Head of US Patient Advocacy & Government Affairs, as the Associate Director, US Patient Advocacy, you will develop and execute key advocacy strategies to strengthen CSL Behring's engagement with patient and non-government stakeholders in the US. You will focus on implementing advocacy initiatives, manage partnerships, and ensure alignment with business priorities across therapeutic areas. You can be based out of our King of Prussia, PA corporate headquarters or our Washington, D.C. office. This is a hybrid role, which offers a combination of an onsite and remote work schedule. #LI-hybrid The Role: - Analyze stakeholder landscape in specific key therapeutic areas relevant to CSL Behring business and assess partnership opportunities. - Implement and manage strategies to build CSL Behring profile and impact with key patients and other non-government stakeholders in the US relevant to the success of our portfolio; collaborate with US PAGA and Commercial organizations to implement partnerships and collaborations. - Coordinate cross-functional participation with key patients and other non-government stakeholders ensure strategic alignment, optimization of investments and tracking of outcomes. - Support development of public affairs content to maximize CSL Behring leadership to support mutual priorities with the advocacy community. - Support creation of advocacy content, including messaging, briefing materials, and communications for campaigns. Your Skills & Abilities: - Bachelor's degree in public affairs, communications, policy, or related field; advanced degree preferred. - Approximately 7 years of experience in healthcare public affairs, advocacy, or related fields. - Proven ability to manage advocacy projects and partnerships with patient and non-government stakeholders. - Strong project management skills and ability to work cross-functionally. - Excellent communication and relationship-building skills. About CSL Behring CSL Behring is a global biotherapeutics leader driven by our promise to save lives. Focused on serving patients’ needs by using the latest technologies, we discover, develop and deliver innovative therapies for people living with conditions in the immunology, hematology, cardiovascular and metabolic, respiratory, and transplant therapeutic areas. We use three strategic scientific platforms of plasma fractionation, recombinant protein technology, and cell and gene therapy to support continued innovation and continually refine ways in which products can address unmet medical needs and help patients lead full lives. CSL Behring operates one of the world’s largest plasma collection networks, CSL Plasma. Our parent company, CSL, headquartered in Melbourne, Australia, employs 32,000 people, and delivers its lifesaving therapies to people in more than 100 countries. Our Benefits For more information on CSL benefits visit How CSL Supports Your Well-being | CSL. You Belong at CSL At CSL, Inclusion and Belonging is at the core of our mission and who we are. It fuels our innovation day in and day out. By celebrating our differences and creating a culture of curiosity and empathy, we are able to better understand and connect with our patients and donors, foster strong relationships with our stakeholders, and sustain a diverse workforce that will move our company and industry into the future

Title: Director State Government Affairs Location: US, Remote time type Full time job requisition id R-277962 CSL Behring is a global biotechnology leader, guided by a promise to save and improve lives. Millions of people around the world are living with rare and serious medical conditions. CSL Behring is committed to delivering medicines that improve their lives. With operations in 35+ nations and ~ 30,000 employees worldwide, CSL is inspired to develop and deliver a broad range of lifesaving therapies to treat disorders such as hemophilia and primary immune deficiencies, and vaccines to prevent influenza. Our therapies are also used in cardiac surgery, organ transplantation and burn treatment. CSL is the parent company of CSL Behring, CSL Plasma, CSL Seqirus and CSL Vifor. CSL Behring is a global leader in the protein biotherapeutics industry, focused on bringing to market biotherapies used to treat serious and often rare conditions Could you be our next Director State Government Affairs, Southeast? The job is located in the Boca Raton, FL or Holly Springs NC area. Will consider other locations in the southeast. You will report to the Senior Director of State Government Affairs. You will be the key point of contact for government officials and stakeholders on state legislative and government policy matters that affect CSL Behring in the Southeast US region. You will have a proven ability to prioritize state activity and a demonstrated understanding of how government actions affect our patients and company operations. You will represent the company and its facilities in the Southeast US region regarding public policy concerns and is responsible for state legislative and state regulatory policy interactions. Collaboration with internal departments—such as market access, government reporting, reimbursement, corporate accounts, communications, marketing, sales, and our CSL Plasma business unit—will be essential, and the Director will be responsible for leading team efforts to assess and address policy issues impacting access to care and business operations in the assigned region. The Director will serve as the company liaison on policy matters with state patient advocacy organizations, trade associations, state medical societies and other groups with complementary policy goals. - Represent CSL Behring and serve as key point of contact for public officials in the assigned region, developing and maintaining relationships with members of state legislatures, committee staff, administrative and regulatory officials, and identifying legislative and administrative champions to advocate on issues affecting CSL Behring. Represent CSL Behring before various state legislative committees, agencies, etc. with regard to CSLB priorities. - Provide legislative strategy and regulatory analysis in addition to political analysis and strategy. Draft legislation, provide technical corrections, and develop support for priorities. Must be able to provide clear, relevant and succinct analysis and guidance to CSLB leadership and cross-functional teams. - Represents our site operations throughout the Southeast region. - Support the growth of CSL Plasma by identifying and developing public official champions and advancing strong public policy that supports plasma donation. Assess and address legislative and state regulatory issues affecting the CSL Plasma network. - Support CSL’s product portfolio by creating and implementing action plans to advance state legislative and regulatory initiatives that allow for access to CSLB therapies. Specifically, advocate for Medicaid policies to ensure patient access to CSL Behring therapies. Collaboration with internal teams is essential, including market access, corporate accounts, reimbursement, contracting, communications, and others. Ability to lead cross-functional discussions, develop and implement action plans, build grass roots support, and communicate status updates and results to diverse stakeholders. - Develop and execute relationship strategies for allies and patient advocacy organizations to advance advocacy initiatives. Build and maintain grassroots coalitions, serving as key point of contact for policy and advocacy. Coordinate with other CSLB departments with responsibilities related to patient group outreach, and work with Policy, Advocacy, and Government Affairs team on positioning CSL Behring’s state advocacy efforts, determining strategies and tactics in assigned states that support CSL Behring’s commitment to state advocacy. - Prepare written summaries of legislation, government action, and analysis of issues for a range of audiences, including corporate leadership, patient advocacy organizations, and other stakeholders. Develop concise and insightful presentations for patient advocacy organizations and contribute articles as needed to corporate publications and communication channels. Ability to express major points in writing while translating complex topics into lay language is essential. - Represent CSL Behring and participate in state affairs committees for trade associations where CSL Behring has membership (PhRMA, BIO, state Biotech Associations, Chambers, etc.) - Work and contribute as a team player by sharing best practices, communicating relevant insights on issues and intelligence, leading special projects, and coordinating with team members to ensure CSL Behring State Government Affairs coverage of key meetings, events, and activities. - Manage the business relationship and direct key activities of contract consultants in designated states and/or projects in order to advance our policy objectives. QUALIFICATIONS: - Bachelor’s degree required (advanced degree preferred) in public policy, government, political science or related field. - 7+ years’ experience preferred, with demonstrated knowledge of the legislative and regulatory process, particularly in the Southeast US region. - Previous experience in government affairs or state government is necessary, with state legislative experience desirable. - Previous advocacy experience with pharmaceutical/biotech, trade associations or patient advocacy organizations is also highly desirable. - Business acumen: understands the life sciences industry and how current and potential policies, trends and practices could affect the industry. - Customer focus: able to establish and maintain effective relationships with internal and external customers and gain their trust and respect. About CSL Behring CSL Behring is a global biotherapeutics leader driven by our promise to save lives. Focused on serving patients’ needs by using the latest technologies, we discover, develop and deliver innovative therapies for people living with conditions in the immunology, hematology, cardiovascular and metabolic, respiratory, and transplant therapeutic areas. We use three strategic scientific platforms of plasma fractionation, recombinant protein technology, and cell and gene therapy to support continued innovation and continually refine ways in which products can address unmet medical needs and help patients lead full lives. CSL Behring operates one of the world’s largest plasma collection networks, CSL Plasma. Our parent company, CSL, headquartered in Melbourne, Australia, employs 32,000 people, and delivers its lifesaving therapies to people in more than 100 countries. You Belong at CSL At CSL, Inclusion and Belonging is at the core of our mission and who we are. It fuels our innovation day in and day out. By celebrating our differences and creating a culture of curiosity and empathy, we are able to better understand and connect with our patients and donors, foster strong relationships with our stakeholders, and sustain a diverse workforce that will move our company and industry into the future.

Title: Executive Assistant, Tech Ops Location: APAC, AU, Victoria, Melbourne, CSL Limited Melbourne Full time job requisition id R-278135 Job Description: Under the direction of senior leadership, the Executive Assistant provides comprehensive administrative and organizational support to leadership within Tech Ops. This role includes managing complex calendars, coordinating meetings and events, and handling domestic and international travel arrangements. The Executive Assistant ensures meeting readiness, manages individual expense reporting, and supports special projects as needed. The position requires interaction with a diverse group of internal stakeholders across all levels and locations, as well as external partners and visitors, while maintaining professionalism and confidentiality at all times. This role reports to: Team Lead, Executive Admin Support for `Tech Ops Your Role & Responsibilities Administrative Support: - Provide diversified administrative support to senior leaders and their teams, including word processing, phone coverage, filing, mailings, and document management. - Organize and maintain confidential and time-sensitive materials and files. Calendar & Meeting Management: - Manage calendars and schedule appointments for executives and leadership team members. - Ensure meeting materials are prepared and assist in tracking priorities and deliverables. Event & Project Coordination: - Plan and manage special projects and events, including global meetings and project-related sessions: - Arrange facilities, catering, invitations, and travel for internal and external participants. - Monitor and control event budgets. - Prepare visual presentations and meeting materials as needed. Travel & Expense Coordination: - Coordinate domestic and international travel arrangements and compile itineraries. - Prepare documents for travel-related meetings and process expense reports accurately and promptly. - Reconcile corporate credit card accounts for assigned leaders. Budget & Compliance: - Monitor standard expenditures to ensure activities remain within established budgets. - Manage implementation of legal contracts and agreements, ensuring proper signatures and maintaining organized files. Onboarding & Collaboration: - Support onboarding new hires and collaborate with other administrative professionals to ensure consistent experience. - Serve as a liaison with internal and external stakeholders globally, representing the department professionally and maintaining confidentiality. Your Skills & Experience - High School Diploma or equivalent vocational or technical training, Bachelor’s degree or Technical College degree a plus - 3-5+ years' administrative support experience preferably in within pharmaceutical industry - Advanced skills in Microsoft Office Suite, Adobe Acrobat, and enterprise systems such as Ariba, SAP, and Concur; ability to quickly learn and adapt to new technologies. - Skilled in providing efficient, high-quality assistance to senior leaders - Demonstrated strength in critical thinking, time management, and organizational skills - Willingness to adjust working hours to accommodate multiple time zones when necessary - Strong interpersonal skills with the ability to navigate complex relationships and maintain professionalism. Location: Elizabeth Street, Melbourne Hybrid Working: 3 days in the office About CSL Behring CSL Behring is a global biotherapeutics leader driven by our promise to save lives. Focused on serving patients’ needs by using the latest technologies, we discover, develop and deliver innovative therapies for people living with conditions in the immunology, hematology, cardiovascular and metabolic, respiratory, and transplant therapeutic areas. We use three strategic scientific platforms of plasma fractionation, recombinant protein technology, and cell and gene therapy to support continued innovation and continually refine ways in which products can address unmet medical needs and help patients lead full lives. CSL Behring operates one of the world’s largest plasma collection networks, CSL Plasma. Our parent company, CSL, headquartered in Melbourne, Australia, employs 32,000 people, and delivers its lifesaving therapies to people in more than 100 countries. You Belong at CSL At CSL, Inclusion and Belonging is at the core of our mission and who we are. It fuels our innovation day in and day out. By celebrating our differences and creating a culture of curiosity and empathy, we are able to better understand and connect with our patients and donors, foster strong relationships with our stakeholders, and sustain a diverse workforce that will move our company and industry into the future. Equal Opportunity Employer CSL is an Equal Opportunity Employer. If you are an individual with a disability and need a reasonable accommodation for any part of the application process.

Title: Legal Counsel, Americas Location: Seqirus USA - NJ - Summit time type Full time job requisition id R-279128 Job Description: Come join a company that tackles fascinating problems and find solutions to complex challenges. With deep expertise in influenza science, our team works on cutting-edge research, pioneering technologies to optimize the manufacturing process and improve the effectiveness of influenza vaccines. We operate as one integrated global organisation, drawing together expert staff from different countries to collaborate. Together, we are working on the front line to protect communities from seasonal influenza and global pandemic threats. When you join Seqirus, you join a team dedicated to making a difference in people's lives. It's a feeling of possibility, creativity, and purpose that inspires us every day. The Opportunity: A rare and exciting opportunity has arisen to join our well established Global Seqirus legal team as the Legal Counsel, Americas. Reporting through to the Seqirus Associate General Counsel, Americas, you will be responsible for supporting the region, by prioritising and delivering expert legal support and partnering with internal stakeholders to achieve strategic business objectives. This is a hybrid role, which offers a combination of an onsite and remote work schedule. #LI-hybrid Your responsibilities will include: - Preparing, negotiating and finalising standard form contracting for the Americas region and forming part of the network of counsels supporting this activity globally for Seqirus. The role acts as the primary regional interface between the other counsels supporting standard form contracts, other regional lawyers, and business stakeholders, ensuring consistent, high‑quality, efficient, and user‑focused contracting support across the region and Seqirus business. - Supporting enterprise initiatives such as template generation and harmonisation, process optimisation and contracting innovation promoting good contracting practices. - Providing general legal advice and counsel to clients in the Americas region including commercial, Medical Affairs, Regulatory and Procurement, as well as the manufacturing operations of the Holly Springs, NC manufacturing facility. - Providing legal advice on certain employment law matters and management of employment law matters (in association with other lawyers in the Americas region). - Working with our Company Secretary and Corporate Governance team and Associate General Counsel to support certain subsidiary management activities. - Providing solutions focused and pragmatic legal advice on a range of legal issues including contract interpretation, and compliance with state and federal laws and regulations, including those applicable to the pharmaceutical industry. - Providing support to and working with the Seqirus Compliance Team to advance compliance related activities and initiatives in the Americas region. - Advising the business on challenges and disputes with third parties and provides advice on management of such issues and disputes. To be successful you will have: - J.D. degree. - Admission to legal practice in a state where Seqirus operates, preferably New Jersey. - 2 to 4 years’ experience in a similar legal role, law firm, in-house position or judicial clerkship. - Excellent written and oral communication skills. - Experience working in a fast-paced environment and ability to prioritize work. - Strong business acumen and judgement. - Ability to work autonomously and as part of a broader team. - Ability to work in a cross functional, cross cultural and matrixed environment. About CSL Seqirus CSL Seqirus is part of CSL. As one of the largest influenza vaccine providers in the world, CSL Seqirus is a major contributor to the prevention of influenza globally and a transcontinental partner in pandemic preparedness. With state-of-the-art production facilities in the U.S., the U.K. and Australia, CSL Seqirus utilizes egg, cell and adjuvant technologies to offer a broad portfolio of differentiated influenza vaccines in more than 20 countries around the world. Our Benefits For more information on CSL benefits visit How CSL Supports Your Well-being | CSL. You Belong at CSL At CSL, Inclusion and Belonging is at the core of our mission and who we are. It fuels our innovation day in and day out. By celebrating our differences and creating a culture of curiosity and empathy, we are able to better understand and connect with our patients and donors, foster strong relationships with our stakeholders, and sustain a diverse workforce that will move our company and industry into the future.

Title: Senior Director, Global Ethics And Compliance Lead Location: NC, NJ USA Full time job requisition id R-279156 Come join a company that tackles fascinating problems and finds solutions to complex challenges. With deep expertise in influenza science, Seqirus works on cutting-edge research and pioneering technologies to optimise manufacturing processes and improve influenza vaccines. We operate as one integrated global organisation, drawing together expert staff from different countries to collaborate. Together, we are working on the front line to protect communities from seasonal influenza and global pandemic threats. The Opportunity: A rare and senior opportunity has arisen to join Seqirus Legal as the Ethics & Compliance Lead. Reporting to the General Counsel, Seqirus, you will be responsible for developing, embedding and continuously improving Seqirus’ global Ethics & Compliance (E&C) framework across all functions and regions. You will partner with senior leaders to identify and manage compliance risks, establish effective controls and assurance, and take a solutions focused approach to drive the ongoing development of an ethics and compliance risk aware organization. This is a hybrid role, which offers a combination of an onsite and remote work schedule. #LI-hybrid Your responsibilities will include: - Developing, establishing and managing the strategic framework, execution cadence and ongoing updates of the global Ethics & Compliance (E&C) framework for Seqirus, ensuring compliance with applicable (non-GxP) laws, regulatory requirements, policies and procedures. - Ensure alignment of the Seqirus E&C Framework to the company’s risk management frameworks and evaluates significance of each ethics and compliance related risk in the context of the company’s risks and key goals. - Providing solutions-focused and business enabling Ethics & Compliance risk advice and guidance to the business, including supporting risk identification, management, controls and mitigations and advising on impacts from regulatory and business changes. - Defining and implementing a global Seqirus Ethics & Compliance program across regions with the support of relevant regional leads, including training, Speak Up/hotline matters, investigations, third party due diligence, regional SOPs, periodic risk assessments, gap analyses and audit programs. This role will include providing primary Ethics & Compliance support for the Americas region too. - Developing, reviewing and implementing compliance policies, SOPs, guidance and tools, and establishing a global repository of Ethics & Compliance information that is kept current and accessible. - Leading Seqirus compliance meetings and deep-dive sessions into key compliance risk areas; developing metrics/KPIs and monitoring Speak Up investigations and regulatory issues. - Collaborating closely with Enterprise Risk and Monitoring & Assurance stakeholders to support Ethics & Compliance reporting, governance and risk-based monitoring and testing. - Identifying opportunities to strengthen Ethics & Compliance capability (including technology, in collaboration with IT), and implementing improvements in accordance with agreed plans. - Leading and developing the Seqirus Ethics & Compliance team, including forward-looking resource planning, role modelling of company values and capability development across geographies. To be successful you will have: - Bachelor’s degree in Business, Risk Management or Law (advanced degree preferred). - 10+ years’ international corporate experience in Compliance and risk management, including significant Ethics & Compliance program leadership. - 5+ years’ experience in the pharmaceutical, life sciences, biotech or medical device industry, with strong knowledge of relevant codes of practice. - Demonstrated ability to identify emerging risks and trends, think strategically about complex risk issues, and deliver pragmatic, solutions-oriented and business enabling advice. - Experience driving and overseeing complex projects to successful completion in global, cross-functional and matrixed environments. - Strong stakeholder influencing, communication, with sound business acumen and judgment. - Strong key strategic and business partnering skills and fosters a solution focused, pragmatic and business empowering approach to all E&C related matters. - Unleashes outcomes and creates an environment of decision making and appropriate risk taking - Leadership experience in managing and developing employees across multiple global locations. - Ability to work in a cross-functional, cross-cultural matrixed environment - Commitment to being part of a global team, including required meetings across different time-zones. - Ability and willingness to travel to other company sites globally. About CSL Seqirus CSL Seqirus is part of CSL. As one of the largest influenza vaccine providers in the world, CSL Seqirus is a major contributor to the prevention of influenza globally and a transcontinental partner in pandemic preparedness. With state-of-the-art production facilities in the U.S., the U.K. and Australia, CSL Seqirus utilizes egg, cell and adjuvant technologies to offer a broad portfolio of differentiated influenza vaccines in more than 20 countries around the world. You Belong at CSL At CSL, Inclusion and Belonging is at the core of our mission and who we are. It fuels our innovation day in and day out. By celebrating our differences and creating a culture of curiosity and empathy, we are able to better understand and connect with our patients and donors, foster strong relationships with our stakeholders, and sustain a diverse workforce that will move our company and industry into the future.

Title: Sr. Director, Intellectual Property Lead Locations: Seqirus USA - NJ - Summit APAC, AU, Victoria, Melbourne, CSL Limited Melbourne Seqirus USA - NC - Holly Springs time type Full time hybrid job requisition id R-279101 Job Description: The Opportunity: Reporting to the General Counsel, Seqirus, as the Intellectual Property Lead, you will have significant responsibility and impact. You will be instrumental in forming strategic partnerships with the respective business leads/TA leads. You will lead and oversee the global management of intellectual property matters (including patents, trademarks, copyright, contentious IP matters, regulatory exclusivities and, as relevant, trademarks and other IP rights) as well as provide strategic guidance to advance the IP assets and create commercial business value and commercial security and confidence. In this role, you will be integral to developing, defending and enforcing Seqirus’ global patent and trademark portfolio, developing and enforcing the Seqirus’ Regulatory exclusivities’ portfolio, as well as ensuring compliance with intellectual property laws, thereby supporting the company's broader business objectives. You will lead and support all IP aspects of deals planned and executed by Seqirus. You will partner with the business stakeholders on developing life cycle management and life cycle initiatives which involve IP amongst other things. You will be the primary point of contact for Seqirus management, including the Seqirus General Counsel for all IP related matters (if required). This is a hybrid role, which offers a combination of an onsite and remote work schedule. #LI-hybrid The Role: - Lead the Seqirus IP function, managing a team of patent and trademark professionals and technical specialists supporting products, platform technologies, and innovation pipelines. This role will report to the Seqirus General Counsel. - Strategic oversight of IP litigation and contentious matters relating to Seqirus products, including coordination of strategy, evidence, and settlement positions with internal stakeholders and external counsel across key jurisdictions. - Provide guidance and high-level oversight on trademark and brand protection strategy for Seqirus products, including clearance and use counseling, coordination of filings and maintenance with external counsel, and potential enforcement actions and disputes. - Responsible for developing, managing and delivering on IP strategy for Seqirus, including relating to clinical development, commercial activities, parallel import, exclusivities (regulatory data exclusivity, orphan drug exclusivity, pediatric exclusivity, PTE/SPC), labelling, life cycle management, country support, communications, patent listings, and LoE preparedness. - Overseeing and supporting the prosecution and leading defense of Seqirus intellectual property, including the identification and safeguarding of inventions relating to Seqirus products and activities, management of IP portfolio with respect to pending applications and granted IP rights taking into account national and international law and guidelines. - Key business partner for senior leadership, commercial and R&D divisions in assessing and leading and strategically managing potential IP challenges relating to Seqirus development and commercial products. Strategic lead, oversight and input for IP disputes, including IP office challenges as well as court litigations (infringement and revocation lawsuits) relating to Seqirus products; advising Seqirus General Counsel. - Lead and support IP aspects of Seqirus' deals, including licensing, collaborations, partnerships, supply and distribution agreements and M&A. - Drive cross-functional collaboration across R&D, Commercial, Regulatory, Clinical, Manufacturing, Strategy, and Legal. - Manage external counsel relationships and direct strategy for disputes, oppositions, litigations, and enforcement matters. Your Skills & Abilities: - Master’s degree in life sciences discipline (chemistry, biochemistry, biotechnology) or a related field, preferably a PhD, or equivalent experience in scientific research. - Qualified Patent Attorney or IP lawyer admitted to practice in the US, Europe or Australia or equivalent legal qualifications and experience in Intellectual Property. - At least 12 years' post-qualification experience in Intellectual Property. - At least 5 years of experience with life science technologies and operations of in-house IP teams with a background in a technical field relevant to Seqirus. - Experience managing or supervising IP litigation (e.g., patent and/or trademark disputes, oppositions, and related proceedings), including instructing and overseeing external counsel. - Experience with trademark matters (e.g., clearance and use advice, portfolio strategy, filings/maintenance managed via outside counsel, and enforcement or dispute resolution) is strongly preferred. - Proven experience in managing an in-house IP team, preferably in pharmaceutical or biotech field. - Proven experience in due diligence, life cycle management, IP challenges and/or negotiations. - This role may require travel, especially to Seqirus sites in Europe, US and Australia and will involve working across different time zones. About CSL Seqirus CSL Seqirus is part of CSL. As one of the largest influenza vaccine providers in the world, CSL Seqirus is a major contributor to the prevention of influenza globally and a transcontinental partner in pandemic preparedness. With state-of-the-art production facilities in the U.S., the U.K. and Australia, CSL Seqirus utilizes egg, cell and adjuvant technologies to offer a broad portfolio of differentiated influenza vaccines in more than 20 countries around the world. Our Benefits For more information on CSL benefits You Belong at CSL At CSL, Inclusion and Belonging is at the core of our mission and who we are. It fuels our innovation day in and day out. By celebrating our differences and creating a culture of curiosity and empathy, we are able to better understand and connect with our patients and donors, foster strong relationships with our stakeholders, and sustain a diverse workforce that will move our company and industry into the future.

Lead statistical strategy and methodologies for clinical development, ensuring robust data analysis and regulatory submissions. Collaborate with cross-functional teams to maximize program success and effectively communicate clinical results.

Lead the design and execution of clinical strategies, ensuring alignment with regulatory standards while overseeing the Clinical Development Team and maintaining high-quality scientific oversight throughout clinical programs.

Title: Area Sales Manager , Nephrology Nashville, TN Location: Americas, US, Remote,CSL Vifor Job Description: At CSL, we use our skills, to offer solutions in iron deficiency, nephrology, and cardio-renal therapies, so we can help patients around the world live better, healthier lives. This is why we come to work every day. Are you empowered to create a better world, and be part of life changing work? As a global pharmaceutical company, we offer the chance to be part of a worldwide team, where passion and commitment are met with opportunities for professional and personal development. Responsibilities - As the Area Sales Manager, you will report into the Regional Business Manager, executing all aspects of sales, market development, and strategic planning for company products. - You will engage with health care professionals involved in the treatment of renal patients in key practice settings, office, hospital, and dialysis. - Daily travel and work within your assigned territory boundaries. - Territory Covers: Tennessee (Nashville, Memphis, Chattanooga, Jackson) Kentucky (Louisville, Lexington, Paducah, Ashland), Ohio (Cincinnati) and Alabama (Birmingham and Huntsville) and surrounding areas - Call on and engage with Nephrologists, health systems, and dialysis organizations and their staff to promote portfolio of company products - Sell the benefits of company products to all key customers, including physicians, nurses, renal dietitians, pharmacists, hospitals, and others as assigned - Demonstrate advanced disease state knowledge and promote product knowledge of company products, competitive products, and renal specialties - Establish positive and productive relationships among marketplace networks within the territory - Analyze sales performance and adjust business plan and approach accordingly - Maintain up-to-date call records for all field contacts; submit reports and paperwork - Represent a positive and professional image of the company externally and internally - Collaborate with Commercial partners Qualifications - The knowledge necessary to perform the responsibilities of this position are typically acquired through the following combination of education, experience, or the equivalent: Minimum Requirements - Bachelor’s degree - 5+ years’ experience selling in the pharmaceutical industry, highly preferred in Nephrology, Renal, and/or Dialysis - Proven track record as a top sales performer - Demonstrated knowledge of account-based selling - Account management experience navigating in a complex, competitive marketplace Preferred Requirements - Renal, Dialysis, Nephrology, Specialty pharma, Rare Disease, and Hospital sales experience - Experience working within IDN systems is highly preferred About CSL Vifor CSL Vifor is a global partner of choice for pharmaceuticals and innovative, leading therapies in iron deficiency and nephrology. We specialize in strategic global partnering, in-licensing and developing, manufacturing and marketing pharmaceutical products for precision healthcare, aiming to help patients around the world lead better, healthier lives. Headquartered in St. Gallen, Switzerland, CSL Vifor also includes the joint company Vifor Fresenius Medical Care Renal Pharma (with Fresenius Medical Care). The parent company, CSL, headquartered in Melbourne, Australia, employs 32,000 people and delivers its lifesaving therapies to people in more than 100 countries. To learn more about CSL, CSL Behring, CSL Seqirus and CSL Vifor visit https://www.csl.com/ and CSL Plasma at https://www.cslplasma.com/. Our Benefits For more information on CSL benefits visit How CSL Supports Your Well-being | CSL. You Belong at CSL At CSL, Inclusion and Belonging is at the core of our mission and who we are. It fuels our innovation day in and day out. By celebrating our differences and creating a culture of curiosity and empathy, we are able to better understand and connect with our patients and donors, foster strong relationships with our stakeholders, and sustain a diverse workforce that will move our company and industry into the future. To learn more about inclusion and belonging visit https://www.csl.com/careers/inclusion-and-belonging Equal Opportunity Employer CSL is an Equal Opportunity Employer. If you are an individual with a disability and need a reasonable accommodation for any part of the application process, please visit https://www.csl.com/accessibility-statement.