Associate Principal Scientist - ADME

About Us: this is who we are

At Cyprotex US, an Evotec company, we believe that curiosity is the spark that drives innovation and success. As a forward-thinking team, we thrive on challenging the status quo, learning from each other, and pushing the boundaries of what’s possible. We're on a mission to create a place where curiosity isn't just encouraged—it’s celebrated. Are you someone who asks questions, seeks answers, and isn't afraid to go deeper? #BeCureious with us and see where your curiosity can take you!

Cyprotex US specializes in ADME-Tox and Biosciences including both in vitro (laboratory experiments) and in silico (computer modelling) approaches. Cyprotex was founded in 1999. The Company serves the Pharmaceutical and Biotech, Cosmetics/Personal Care and Chemicals Industries as well as academia and not-for-profit organizations. Over 1700 organizations trust Cyprotex for their ADME-Tox and Bioscience research needs.

The Role: Your challenge …in our journey

We’re looking for a passionate and curious Associate Principal Scientist to join our team. If you’re excited by new challenges, solving complex problems, and learning every step of the way, you might just be the perfect fit. In this role, you’ll have the opportunity to drive impactful projects, collaborate with bright minds, and explore uncharted territories.

As an Associate Principal Scientist at Cyprotex, you'll have the freedom to ask the hard questions, think outside the box, and find creative solutions that push us forward. It’s a role where your curiosity will fuel both your personal growth and the success of the team.

What You'll Do:

• Perform routine in-vitro toxicology assays
• Responsible for planning, performing and reporting in vitro TOX studies for discovery and development stage compounds.
• Actively participate in experimental design, perform experiments as well as critically analyze, interpret and report the data to design next steps.
• Ability to perform high-impact as well as high throughput studies to completion in a fast paced environment, while managing multiple projects to meet the timelines
• Provides scientific knowledge and responsible in establishing new TOX assays as well as contribute to the continuous improvement of the current TOX assays
• Guide junior scientists within the department
• Assist in data analysis and interpretation
• Laboratory support including ordering, equipment calibration and validation Working to a high standard and adhering to our Quality System
• Work closely with the Project Managers to ensure the requirements of our clients are met
• Assist in running and maintaining robotic systems to support processes.
• Perform Quality Review of peer data and assist in consolidating assay control and validation criteria
• Work closely with the Project Managers to ensure the requirements of our clients are met

Who You Are:

• PhD in a scientific relevant field with at least 3 years of related experience in contract research organizations, pharmaceutical industries or academia.
• An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
• Experienced in High Content Assay development
• Experienced in Imaging based and MEA based assays
• Experienced in drug discovery/development
• Broad understanding of TOX
• Experienced in cell based or biochemical assays.
• Ability to work in a team environment, remaining attentive to ideas, recognizing responsibilities, and actively participating with others to accomplish assignments and achieve desired goals.
• Excellent oral and written communication skills.
• Knowledge and proficiency with Microsoft Word and Outlook.
• Strong attention to detail.
• Ability to communicate with peers and all levels of management.
• Ability to manage time and works independently.