Associate Principal Scientist - in vitro Tox

Evotec•Princeton, NJ

10h

About The Position

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.

Requirements

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

Responsibilities

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