Jobs · Healthcare

Director, Translational Immunology

Travere Therapeutics · United States · 2 days ago
RemoteRemoteHealthcare$189k–$246k/yrFull-time

Responsibilities

  • Serve as the immunology lead supporting a late-stage clinical development program.
  • Contribute to the development and execution of nonclinical and translational strategies aligned with program team objectives.
  • Partner with cross-functional teams to support program governance, development planning, and scientific decision-making.
  • Assess emerging scientific, clinical, and competitive developments relevant to assigned program and associated strategy.
  • Contribute to the identification and evaluation of new therapeutic opportunities in rare disease for the assigned program that may provide clinical benefit.
  • Develop translational strategies linking mechanism of action, target engagement, pharmacodynamic activity, and clinical outcomes.
  • Support identification and implementation of mechanistic, pharmacodynamic, predictive, and response biomarkers.
  • Collaborate with cross-functional teams to support implementation of biomarker strategies and data interpretation throughout development.
  • Contribute to scientific publications, presentations, and external communications.
  • Collaborate with Regulatory and nonclinical colleagues to support regulatory submissions and health authority interactions.
  • Interpret pharmacology, toxicology, and translational data in the context of clinical development and regulatory objectives.
  • Support preparation and review of investigator brochures, briefing documents, regulatory submissions, and other development-related documents.
  • Ensure research and translational activities are aligned with development plans and regulatory expectations.
  • Lead scientific interactions with CROs, academic collaborators, consultants, and key opinion leaders.
  • Design, oversee, and contribute to interpretation of externally conducted translational and mechanistic nonclinical studies.
  • Represent Travere at scientific meetings, conferences, and external collaborations.
  • Identify and build productive scientific relationships that advance understanding of disease biology and therapeutic mechanisms.
  • Contribute to building immunology and translational science capabilities within the Research and Nonclinical Development organization.
  • Mentor colleagues and provide scientific leadership across programs and functions.
  • Foster a culture of scientific excellence, collaboration, innovation, and continuous learning.
  • Demonstrate the potential and desire to assume increasing scientific leadership responsibilities as the organization grows.
  • Provide deep scientific expertise in B-cell biology, adaptive immunity, and innate immune signaling.
  • Evaluate disease mechanisms and therapeutic opportunities in immune-mediated and rare diseases.
  • Integrate mechanistic biology, translational science, and clinical observations to inform development strategies.
  • Serve as an internal subject matter expert in immunology and immune-mediated disease biology.
  • Maintain awareness of advances in disease biology, therapeutic targets, and emerging technologies relevant to immunology and translational medicine.

Requirements

  • Bachelor’s Degree in Life Science or other related discipline required.
  • PhD, MD, PharmD, or equivalent advanced degree in Immunology, Cell Biology, Molecular Biology, Pharmacology, or a related scientific discipline preferred.
  • Minimum 10 years of relevant experience in the biopharmaceutical industry required; or 6 years with PhD, MD, PharmD, or equivalent.
  • Demonstrated expertise in immunology, with strong knowledge of B-cell biology and immune signaling pathways.
  • Experience supporting clinical-stage drug development programs.
  • Experience translating mechanistic biology into development strategies and clinical applications.
  • Experience leading externally conducted research through CROs, academic collaborators, and consultants.
  • Working knowledge of regulatory requirements and expectations for nonclinical support of clinical development programs.
  • Experience contributing to regulatory submissions, investigator brochures, briefing documents, or related development activities.
  • Demonstrated ability to work effectively in cross-functional, matrixed organizations.
  • Prior experience leading scientific initiatives, projects, or multidisciplinary teams.
  • Excellent communication, presentation, and influencing skills.
  • Scientific curiosity, intellectual rigor, and commitment to improving outcomes for patients with serious diseases.
  • Ability to thrive in a collaborative, fast-paced, virtual biotechnology environment.

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