About The Position

At Cyprotex US, an Evotec company, the team believes that curiosity drives innovation and success, encouraging a culture of questioning and problem-solving. Cyprotex US specializes in ADME-Tox and Biosciences, utilizing both in vitro (laboratory experiments) and in silico (computer modelling) approaches, serving various industries including Pharmaceutical and Biotech, Cosmetics/Personal Care, Chemicals, academia, and not-for-profit organizations since its founding in 1999. Over 1700 organizations trust Cyprotex for their ADME-Tox and Bioscience research needs. The company is seeking a passionate and curious Associate Principal Scientist to join their team. This role involves driving impactful projects, collaborating with bright minds, and exploring uncharted territories. The Associate Principal Scientist will have the freedom to ask challenging questions, think creatively, and find solutions that advance the company's goals, fostering both personal growth and team success.

Requirements

  • PhD in a scientific relevant field with at least 3 years of post PhD experience in contract research organizations, pharmaceutical industries or academia.
  • Industry/academic experience in cell biology and electrophysiology and a strong record of scientific achievement
  • Experience in drug discovery/development, especially MEA 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 with peers and all levels of management
  • Knowledge and proficiency with Microsoft Word and Excel
  • Strong attention to detail
  • Ability to manage time and work independently
  • Ability to train and mentor junior scientists
  • Broad understanding of Toxicology, electrophysiology, and cell biology

Nice To Haves

  • Expertise in electrophysiological assays with Microelectrode Array for cardiac and neuro assays is highly desired

Responsibilities

  • Perform routine in-vitro toxicology assays, with a focus on Microelectrode Array (MEA)
  • Responsible for planning, performing and reporting in vitro Toxicology 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
  • Perform Quality Review of peer data and assist in consolidating assay control and validation criteria

Benefits

  • discretionary annual bonus
  • comprehensive benefits to include Medical, Dental and Vision
  • short-term and long-term disability
  • company paid basic life insurance
  • 401k company match
  • flexible work
  • generous paid time off
  • paid holiday
  • wellness and transportation benefits

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What This Job Offers

Job Type

Full-time

Career Level

Senior

Education Level

Ph.D. or professional degree

Number of Employees

501-1,000 employees

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