Gilead focuses on developing and delivering medications that advance the treatment of life-threatening diseases.
The commercial success of our portfolio of 21 products provides us with the resources to generate new clinical data defining their profiles and supports the development of new therapeutic advancements. Today, our research and development effort is the largest it has ever been evaluating compounds with the potential to become the next generation of innovative therapies for HIV, liver disease, serious respiratory and cardiovascular conditions, cancer and inflammation.
Here you will work in a fast-paced environment and on a growing, well-respected team whilst having plenty of opportunities for career advancement. Be part of an organisation that has helped millions of people around the world live healthier, more fulfilling lives.
Make an impact. As a member of the Biostatistics team, you will work on all phases of clinical trials, from inception to filing NDAs to post-approval studies. That means being involved in writing sections of case study reports, publications, abstracts, posters and more. It’s a collaborative culture where your contributions matter and you are regularly exposed to new methodologies, making it a dynamic environment to learn the drug development process.
“Working one year here at Gilead is equal to three years at any other company; you have the opportunity to learn so much.”Ya-Pei, Senior Manager, Biostatistics
Work fast and efficiently, collaborate and improve upon the existing infrastructure. On the Statistical Programming team, we strive to have well-defined, standardized operational processes across all therapeutic areas. Our Study Data Tabulation Model (SDTM) group has implemented procedures to ensure Gilead is CDISC compliant and well-positioned for the future. You will join other highly skilled team members in this fast-paced environment, working on exciting projects and refining best practices.
“Every day someone impresses me at Gilead with their intelligence and dedication. It is the most exciting team and company that I’ve ever been a part of.”Jay, Senior Manager, Statistical Programming
Help make us better at what we do. As a member of the Clinical Data Management team, you will work on every aspect of drug development, from protocols to international submissions. From writing clinical study reports and regulatory submissions to working on cross-functional teams, you will have opportunities to grow. And you’ll do it on an experienced team with dynamic management that values proactivity.