Principal Scientific Advisor (REMOTE)

Lifelancer
Any Location, MA
Category Research
Job Description
We are seeking an experienced nonclinical drug development professional to serve as a Principal Scientific Advisor within our Discovery and Safety Assessment business units. The Scientific Advisory Services team is hiring an experienced professional with expertise in establishing effective scientific and regulatory strategies to advance new medicines through the various stages of the development process.

Requirements

  • Master’s degree or PhD in relevant discipline (toxicology, pharmacology, biology, immunology, etc.)
  • Minimum 15 years’ experience in pharmaceutical/biotech sector, nonclinical contract research or consulting including at least 10 years nonclinical drug development experience
  • Must have direct experience in regulated toxicology and drug development
  • Certification/Licensure: DABT, DACVP or European Registered Toxicologist preferred
  • Applied understanding of regulatory requirements for the conduct of nonclinical safety assessment studies including Testing Facility SOPs and the Good Laboratory Practices (GLPs)
  • Deep understanding of relevant regulatory guidance documents is essential
  • Demonstrated leadership skills in support of intra- and interdepartmental initiatives, client/external interactions, and business development
  • Proficiency in the use of standard software including Microsoft Excel, Word, PowerPoint, etc. and standard laboratory calculations

Benefits

  • bonus/incentives based on performance
  • 401K
  • paid time off
  • stock purchase program
  • Health and wellness coverage
  • employee and family wellbeing support programs
  • work life balance flexibility
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