Job Opening: Medical Director/Senior Medical Director

Job Summary

Auron Therapeutics is developing next-generation targeted cancer therapies by identifying and targeting the drivers of the disrupted cell states found in cancer, and reverting cancer cells from a plastic, proliferative cell state to a more mature, non-proliferative cell state. Using its AURIGIN™ platform, Auron is building a pipeline of small molecule targeted therapies, led by AUTX-703, for the treatment of both solid tumors and hematologic malignancies.

Key Reponsibilities

Collaboratively lead medical aspects of our clinical development programs, from early to late-stage trials.
Partner with Clinical Development, Regulatory, Biostats, Program Leadership, Pharmacovigilance, Research and other colleagues to guide strategy for Auron’s oncology pipeline from pre-IND to pivotal development.
Educate and advise clinical site investigators and study staff to support study interest, enrollment and optimal study conduct.
Contribute to the development of clinical documents, including protocols, investigator brochures, clinical study reports, medical monitoring plans, etc.
Oversee medical monitoring activities to ensure patient safety and data integrity and facilitate Safety Review Committee meetings.
Partner with Pharmacovigilance colleagues to oversee safety event reporting, review of safety narratives, etc.
Review and analyze clinical trial data; prepare reports and presentations for internal and external stakeholders.
Contribute to US and Global (as needed) regulatory agency submissions and meetings.
Build relationships with KOLs to bring expertise to Auron programs and facilitate Advisory Board meetings as needed.
Stay current on relevant scientific advancements and clinical trial landscape in oncology.
Represent the company at medical conferences and scientific meetings.

Your Background

MD or DO degree; clinical experience and/or board certification in Medical Oncology or Hematology/Oncology a plus
Minimum 5+ years of experience in the pharmaceutical or biotechnology industry with broad experience leading and managing clinical trial programs from early to late stage.
Pivotal study management and global submission (e.g., NDA, MAA) experience a plus
Excellent understanding of and experience with clinical trial design (e.g., phase 1, 2 and 3, dose escalation and/or optimization, randomized), regulatory requirements, and Good Clinical Practice (GCP) principles.
Must be comfortable and effective BOTH as an individual contributor and collaborative team player in a fast-paced and dynamic small-biotech environment, adapting as the company grows.
Excellent writer and oral communicator; strong interpersonal, leadership and people-management skills.
Flexible and creative thinker and problem-solver.
Ability to work independently and manage multiple priorities in a fast-paced environment.

Medical Director/Senior Medical Director

Job Summary

Key Reponsibilities

Your Background

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Medical Director/Senior Medical Director

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