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Driven by our promise to help patients lead full lives. Social Guidelines: https://bit.ly/3Bs17Ra
As a Principal Scientist in CSL’s cardiovascular and renal translational research team, Christopher builds and refines research models that give our potential therapeutic treatments their best shot at being successful.
Read Christopher’s story here: CSL.com/people-powering-science
At CSL, great science doesn’t start with molecules. It starts with people.
Today we’re launching a series of stories that bring to life the people, motivations and determination behind our research.
Learn more about the people powering our science: csl.com/people-powering-science
02/06/2026
We’re committed to more than medicine — we’re committed to people.
CSL teams work tirelessly to improve life for patients with chronic conditions like kidney disease, helping them live fuller, healthier lives.
If you want a career where your skills make a real difference, join us and help shape the future of healthcare: csl.com/careers
What does a day at CSL look like?
For our teams, it’s a balance of collaboration, focus and purpose-driven work – each moment contributing to something bigger.
Take a look inside a typical day and see how our people are making an impact.
Explore careers: csl.com/careers
Lisa Butler, President & CEO of the GBS-CIDP Foundation International, sat down with Emma Hatcher, Director of U.S. Patient Advocacy at CSL, to explain Chronic Inflammatory Demyelinating Polyneuropathy ( ).
CIDP, an autoimmune disease affecting the peripheral nervous system, causes extreme weakness and profound fatigue. These unpredictable symptoms can disrupt daily life, turning routine activities into significant challenges for those living with the condition.
Learn more: https://bit.ly/4f0Q070
20/05/2026
Every safe, effective therapy starts with clinical trials—and they wouldn’t happen without the people who step forward to participate, or the clinical research professionals who bring these studies to life.
Thank you to the people who participate in clinical research studies to advance new medicines and everyone working to turn scientific discovery into real-world impact.
18/05/2026
The experience of hereditary angioedema (HAE) reminds us that progress in rare disease is about more than science alone.
Professor Konrad Bork, a pioneer in HAE who has shaped the field for more than four decades, shared his perspective on the evolution of HAE care, the remaining challenges and his experience of HAE.
With HAE Day taking place in May, we want to recognize the role of the healthcare community in helping improve understanding of this rare disease, support earlier recognition, and drive progress in care.
Read the full interview here: https://www.csl.com/we-are-csl/vita-original-stories/2026/an-hae-pioneer-reflects-on-the-evolution-of-care?utm_source=Social+Media&utm_medium=Facebook&utm_campaign=HAE
18/05/2026
More than 33,000 patients participated in our clinical trials in fiscal year 2025, helping CSL drive innovation and transform lives.
Every breakthrough starts with passionate people working behind the scenes to make a difference.
Be part of a team advancing breakthroughs that improve health worldwide. Discover opportunities: csl.com/careers
Feeling supported makes a difference.
At CSL, we offer wellness days and resources that give our employees time to reset and recharge – so they can bring their best to work and beyond.
Because supporting health starts from within.
Explore careers: csl.com/careers
16/05/2026
The experience of hereditary angioedema (HAE) can be unpredictable, disruptive and difficult for others to fully see.
Melissa shared her HAE story, and the burden of unpredictable, painful and potentially life-threatening swelling attacks.
With HAE Day taking place in May, we’re recognizing the lived reality of HAE and the importance of greater awareness, understanding and support for the community.
To provide further perspective, Professor Konrad Bork, a pioneer in HAE research, shares his expert insights in an interview exploring the importance of how awareness, experience, and collaboration continue to drive progress in rare disease care: https://www.csl.com/we-are-csl/vita-original-stories/2026/an-hae-pioneer-reflects-on-the-evolution-of-care?utm_source=Social+Media&utm_medium=Facebook&utm_campaign=HAE_Melissa
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