Evommune

Evommune

Director, Toxicology

Palo Alto, CA · Director

Sponsorship not specified$226k-$280kDetected 3 days ago
PharmacologyFDA RegulatoryScientific WritingResearchExperimental DesignCommunicationCollaborationRegulatory Affairs

About the role

  • Evommune is seeking an experienced and highly motivated PhD Toxicologist to join the company as Director, Toxicology.
  • The successful candidate will bring strong scientific judgment, hands-on experience managing outsourced toxicology studies, and a solid understanding of regulatory expectations for nonclinical safety assessment.
  • This is a highly collaborative, individual-contributor role that requires both strategic thinking and operational execution in a fast-paced biotechnology environment.

Responsibilities

  • Develop and execute nonclinical toxicology strategies for assigned development programs.
  • Provide scientific guidance on nonclinical safety risks, study design, and program advancement.
  • Design, oversee, interpret, and report exploratory, IND-enabling, and clinical-stage toxicology studies.
  • Manage external contract research organizations, consultants, study directors, and other scientific partners.
  • Partner closely with colleagues in Research, DMPK, Translational Sciences, Clinical Development, Regulatory Affairs, CMC, and Program Management.
  • Support due diligence, portfolio evaluation, and other scientific activities as needed.
  • This individual will provide toxicology strategy and executional support across Evommune's development programs.

Nice to have

  • Experience supporting small molecule programs.
  • Board certification in toxicology, such as DABT.
  • Experience in immunology, inflammation, dermatology, or immune-mediated diseases.
  • Experience supporting programs from candidate selection through early clinical development.
  • Prior experience working in a small or mid-sized biotechnology company.
  • Core Competencies Strong scientific and regulatory judgment.
  • Ability to balance strategic thinking with hands-on execution.
  • Clear and concise communication of complex scientific information.

Compensation

  • $226k-$280k

Benefits

  • Company-sponsored benefits, including comprehensive health, dental, and vision plans, as well as pet insurance.
  • In addition, we offer a 401(k) plan, ample time-off programs, paid parental leave, life insurance, disability insurance, and an employee referral bonus program.
  • Support the preparation of nonclinical sections of regulatory submissions, including pre-IND briefing packages, INDs, clinical trial applications, investigator brochures, and responses to health authority questions.

Equal opportunity

  • equal opportunity employer and will consider all qualified applicants for employment.

This listing is sourced directly from Evommune's careers page and normalized into a canonical job model.