Senior Director, Nonclinical Safety Evaluation

The Senior Director, Nonclinical Safety Evaluation role at Moderna is responsible for providing strategic and operational leadership for Toxicology and Pathology. The role will serve on a leadership team with other nonclinical leaders and partner with cross-functional stakeholders to ensure scientifically rigorous nonclinical safety strategies and data packages to support regulatory submissions.

Requirements

• PhD
• 11 or more years of experience in nonclinical safety assessment activities in pharmaceutical development
• Experience in nucleic acid-based and nanoparticle modalities, immune-modulating therapeutics, oncology, and/or infectious disease vaccine drug development
• Experience in mentoring, coaching, and/or managing others
• Experience applying regulatory guideline knowledge in the conduct of nonclinical safety studies to support regulatory filings
• Direct experience in writing, reviewing, and critiquing nonclinical sections of regulatory submission documents
• Outstanding written and verbal communication skills
• Attention to detail and quality
• Ability to deliver work on time
• Demonstrated ability to work successfully in a fast-paced and dynamic work environment

Benefits

• Best-in-class healthcare coverage
• Voluntary benefit programs to support unique needs
• Holistic approach to well-being
• Fitness, mindfulness, and mental health support
• Family planning benefits
• Generous paid time off
• Savings and investment opportunities
• Location-specific perks and extras