Senior Director, Toxicology

Role Summary:

The Senior Director, Toxicology is a key member of preclinical development teams and be responsible for the strategic planning and execution of nonclinical safety plans of Dyne’s portfolio programs supporting late discovery through first-in-human and proof-of-concept clinical studies of investigational therapeutics consisting of targeting antibodies s conjugated with a variety of oligonucleotide and protein payloads to treat serious neuromuscular diseases. The person in this role must possess an in-depth understanding of regulatory guidance as they pertain to the nonclinical development of novel therapeutics along with documented experience designing and critically evaluating results of exploratory and GLP-compliant toxicology studies. Previous experience in authoring and reviewing nonclinical regulatory documents as well as interactions with regulatory authorities is required. This individual should have experience in the nonclinical safety assessment of therapeutic antibodies and/or oligonucleotides. The ability to work collaboratively with cross-functional teams is critical for this position.

This role is based in Waltham, MA without the possibility of being a remote role.

Primary Responsibilities Include:

• Represent Preclinical Development (PCD) on program teams, providing expertise and guidance in regulatory toxicology
• Design and execute nonclinical safety plans for Dyne candidate therapeutics
• Principal contact to external CROs executing these studies, ensuring studies are conducted in line with the appropriate quality and regulatory standards and guidelines (FDA, CHMP, WHO and GLP)
• Responsible for interpreting toxicology data and communicating results to program teams and senior management
• Responsible for writing appropriate content and submission-ready documentation for the toxicology components of regulatory submissions
• Lead issue-resolution teams, driving the science for investigative and discovery toxicology as needed
• Participate in the design and expansion of Dyne’s 

Education and Skills Requirements:

• PhD and post-doctoral training in toxicology or a related field and/or DVM
• Relevant board certification in toxicology and / or Veterinary Pathology
• 8+ years of experience of nonclinical development experience in a biotech or pharmaceutical setting including direct experience in preparation of toxicology components of regulatory submissions
• Experience in development of toxicology study package to ensure compliance with regulations
• Experience designing and managing studies at contract research organizations
• Experience writing and interpreting toxicology data, including the development of final reports
• Experience in development of new supportive technologies or toxicological approaches
• Experience assessing toxicity of antibody-drug conjugates is a plus
• Expertise in immunology or immunotoxicology is a plus
• Experience in people management is a plus
• Strong written and oral communication, organization and multitasking skills
• Ability to work in a highly collaborative and cross-functional research environment including managing project timelines to meet corporate goals
• Flexibility to function well within a team environment and within condensed timelines
• Ability to verbalize complex study issues and demonstrated problem-solving ability

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