Associate Principal Scientist - In-Vitro Tox - Site Based, Princeton, NJ
Evotec
2 months ago
On-site
Princeton, NJ
Clinical Research and Development
What You'll Do
- Perform routine in-vitro toxicology assays.
- Plan, perform, and report in vitro TOX studies for discovery and development stage compounds.
- Participate in experimental design; perform experiments and critically analyze, interpret, and report data to define next steps.
- Complete high-impact and high-throughput studies in a fast-paced environment while managing multiple projects to meet timelines.
- Establish new TOX assays and contribute to continuous improvement of current TOX assays.
- Guide junior scientists within the department.
- Assist with data analysis and interpretation.
- Provide laboratory support (ordering, equipment calibration and validation) while adhering to the Quality System.
- Work with Project Managers to ensure client requirements are met.
- Assist in running and maintaining robotic systems.
- Perform quality review of peer data; consolidate assay control and validation criteria.
Who You Are (Qualifications)
- PhD in a scientific relevant field with at least 3 years of related experience in contract research organizations, pharmaceutical industries, or academia.
- Equivalent education and experience may be accepted.
- 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.
- Strong oral and written communication skills.
- Knowledge of Microsoft Word and Outlook.
- Strong attention to detail; ability to manage time and work independently.
Benefits
- Discretionary annual bonus; medical, dental, and vision; short- and long-term disability; company-paid basic life insurance; 401(k) company match; flexible work; generous paid time off and paid holidays; wellness and transportation benefits.
- Perform routine in-vitro toxicology assays.
- Plan, perform, and report in vitro TOX studies for discovery and development stage compounds.
- Participate in experimental design; perform experiments and critically analyze, interpret, and report data to define next steps.
- Complete high-impact and high-throughput studies in a fast-paced environment while managing multiple projects to meet timelines.
- Establish new TOX assays and contribute to continuous improvement of current TOX assays.
- Guide junior scientists within the department.
- Assist with data analysis and interpretation.
- Provide laboratory support (ordering, equipment calibration and validation) while adhering to the Quality System.
- Work with Project Managers to ensure client requirements are met.
- Assist in running and maintaining robotic systems.
- Perform quality review of peer data; consolidate assay control and validation criteria.
Who You Are (Qualifications)
- PhD in a scientific relevant field with at least 3 years of related experience in contract research organizations, pharmaceutical industries, or academia.
- Equivalent education and experience may be accepted.
- 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.
- Strong oral and written communication skills.
- Knowledge of Microsoft Word and Outlook.
- Strong attention to detail; ability to manage time and work independently.
Benefits
- Discretionary annual bonus; medical, dental, and vision; short- and long-term disability; company-paid basic life insurance; 401(k) company match; flexible work; generous paid time off and paid holidays; wellness and transportation benefits.