Top Navigation
Global
Choose your region
Don't see your region/country listed? Visit our global website
Related content
Chief Human Resources Officer Stephanie Franklin discusses our unique culture at Vertex and how we bring our culture to life.
Our CEO and President, Reshma Kewalramani shares her thoughts on how Vertex is rethinking work and education in an extremely competitive talent market
Join us as we celebrate 15 years of giving back at Vertex.
In this section
Our scientists don’t see the impossible as an obstacle; they see it as a good place to start
See where our scientific discoveries happen
Volunteers who participate in clinical trials help make new medicines a reality
Information about our Early Access program and how we evaluate requests
Instructions on how to submit a report
We work with the kidney disease community to ensure their voices are represented in all that we do
See how we're engaging with the sickle cell disease community
Discover how we're inspiring and equipping the next generation to love science and pursue a career in STEM
Explore our commitment to limiting our environmental impacts and operating our business in a sustainable manner
Read more about how we operate our business responsibly, and how in 2022 we created more ways to positively impact patients, employees, our communities and the environment
Chief Human Resources Officer Stephanie Franklin discusses Vertex’s inclusive benefits and how they are helping Vertexians.
Our commitment to inclusion, diversity and equity (ID&E) is longstanding and achieving our ambition takes collective action and shared ownership. Learn more about our approach from Vice President of Talent and ID&E Diana Cruz Solash.
Discover more about our relentless efforts to improve the lives of patients, employees and our communities.
Individuals living with severe sickle cell disease report higher exposure to health care prejudice, according to new research by our Health Economics and Outcomes Research (HEOR) team.
Vertex is committed to the sickle cell disease community. Beyond our science, it’s about showing up and locking arms with the community to work together toward meaningful change.
Understanding the real-life impacts of managing SCD and TDT.
Learn how we explore the daily lives of those living with debilitating disease to help inform our mission.
On World Blood Donor Day, hear from two individuals living with sickle cell disease and transfusion-dependent beta thalassemia as they share their stories, shed light on their struggles, and emphasize the impact blood donation has had on their disease and quality of life.
Learn how our teams utilize real-world research to understand the lived impacts of sickle cell disease and beta thalassemia.
The Sickle Cell Disease Partnership is a multistakeholder coalition, launched in June, which works to improve care and access for people living with sickle cell disease. Here, Chief Patient Officer Amit Sachdev discusses the partnership, its goals and the reasons it was founded.