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Be part of Certara’s growing global team of leading experts, make a difference in the world.

Certara has the opportunities you’re looking for to join the teams driving regulatory success for ground breaking medicines!

Experience career growth collaborating with top scientists utilizing cutting-edge tools in order to tackle the toughest challenges in global drug development.

To learn more about Certara’s dynamic culture here. 

Jobs in the United States

We are proud to be an Equal Opportunity Employer, always striving to foster and nurture a culture of diversity and inclusion. The collective sum of our individual differences, life experiences, knowledge, innovation, self-expression, and unique capabilities and talent represents a significant part of not only our culture, but also our reputation and achievement.

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Jobs in the United States
Jobs in Canada

Jobs in Canada

“Here at Certara I have access to key experts, and there is great sharing of knowledge and collective team spirit. We are surrounded by great leaders who are still doing science and inspiring work. Every day we make a difference by pushing the boundaries of science forward for our clients and eventually the patients.”
– Eva Gil Berglund, PhD
Senior Director, Regulatory Strategy
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Jobs in Europe

“Improving public health through model informed drug development (MIDD) is a passion for me. It’s a truly multidisciplinary endeavor bringing together experts here at Certara and our clients. Success is ensuring the right drug discovery and development decisions are made and new medicines are delivered to patients to improve their lives.”
– S.Y. Amy Cheung, PhD
Senior Director, Quantitative Science Strategy
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Jobs in Europe
Jobs in the Asia-Pacific region

Jobs in the Asia-Pacific region

“I joined Certara for the opportunity to work at an innovative organization that is growing and evolving to meet the needs of global regulators and our clients. I love the collaborative, supportive, and flexible environment where I can work to bring meaningful solutions to patients around the globe.”
– Heather Graham
Vice President, Regulatory Writing and Scientific Publications
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