Senior Director, Nonclinical Safety Evaluation

Moderna

Remote
$196,700.00 - $353,400.00; annual discretionary bo...
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Strategic and operational leadership
Toxicology and pathology
Support regulatory submissions
** Moderna is seeking a Senior Director for Nonclinical Safety Evaluation to lead strategic and operational initiatives in toxicology and pathology, particularly for cancer and infectious disease therapies. The role requires extensive experience in nonclinical safety assessment and regulatory submissions, with an emphasis on fostering a collaborative and innovative team culture. **

Job Summary

  • Provide strategic and operational leadership for Toxicology and Pathology, ensuring scientifically rigorous, acceptable, and compliant nonclinical safety strategies and data packages to support regulatory submissions.
  • Manage a high-performing team of Toxicologists and Pathologists, cultivating a culture of innovation, collaboration, excellence, and continuous learning.
  • Serve as a key scientific contributor in regulatory agency interactions and internal governance meetings, presenting nonclinical data package conclusions and their impact on program and clinical/regulatory strategy.

Matching Summary

Match Score: 75

** Moderna is seeking a Senior Director for Nonclinical Safety Evaluation to lead strategic and operational initiatives in toxicology and pathology, particularly for cancer and infectious disease therapies. The role requires extensive experience in nonclinical safety assessment and regulatory submissions, with an emphasis on fostering a collaborative and innovative team culture. **

Salary

$196,700.00 - $353,400.00; Annual discretionary bonus, other incentive compensation, or equity award may be eligible; Best-in-class healthcare coverage, holistic well-being resources, family planning benefits, generous paid time off

Skills & Requirements

Must-have

  • strategic and operational leadership
  • Toxicology and Pathology
  • support regulatory submissions
  • GLP/non-GLP nonclinical safety studies
  • regulatory agency interactions
  • scientific and regulatory writing

Nice-to-have

  • nucleic acid-based and nanoparticle modalities
  • immune-modulating therapeutics
  • cancer antigen therapy
  • infectious disease portfolios
  • fast-paced and dynamic work environment

Key Requirements

  • PhD & 11 or more years of experience
  • Experience mentoring, coaching, and/or managing others
  • Experience applying regulatory guideline knowledge
  • Direct experience writing regulatory submission documents
  • U.S. person eligibility

Work Rights

U.S. person eligibility

Tailored Resume

Cover Letter