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BeOne

Global oncology therapeutics discovery, development, manufacturing

Director, Clinical Biomarkers & Translational Medicine - Oncology, Solid Tumor Portfolio

Clinical Research OperationsConfirmed live in the last 24 hours
Full-time$176.6k - $236.6k /yrRemote

About the Job

Requirements

  • A minimum of five years of pharmaceutical or biotechnology industry experience in oncology drug development, including substantial experience leading clinical biomarker and translational medicine strategies.
  • Demonstrated success supporting biomarker strategy across Phase I–III oncology clinical development.
  • Experience developing biomarker strategies for targeted therapies, immuno-oncology agents, and/or antibody-drug conjugates.
  • Deep expertise in translational oncology and clinical biomarker science.
  • Working knowledge of next-generation sequencing, RNA sequencing, ctDNA, multiplex immunohistochemistry, digital pathology, proteomics, flow cytometry, single-cell technologies, emerging multi-omics approaches, data integration, and computational biology.
  • Strategic scientific leadership and ability to influence multidisciplinary teams in a global matrix environment.
  • Strong scientific judgment and data-driven decision-making.
  • Ability to build productive external scientific collaborations.
  • Strong publication record and recognized scientific credibility within the oncology community.
  • PhD, MD, PharmD, or MD/PhD in Oncology, Molecular Biology, Immunology, Cancer Biology, Pharmacology, or a related scientific discipline.

Responsibilities

  • Lead development and execution of integrated translational medicine and clinical biomarker strategies from First-in-Human through registration for assigned oncology programs.
  • Develop biomarker strategies supporting patient selection and enrichment; pharmacodynamic assessments, including target engagement; mechanism of action and mechanisms of sensitivity and resistance; dose optimization; and prognostic and predictive biomarker development.
  • Ensure biomarker plans are scientifically rigorous, operationally feasible, and aligned with overall clinical development objectives.
  • Integrate and interpret clinical, molecular, pharmacologic, and translational datasets to generate biological insights that inform program strategy, clinical development decisions, and portfolio prioritization.
  • Provide scientific leadership for biomarker-related regulatory activities.
  • Establish and manage strategic collaborations with academic investigators, contract research organizations, central laboratories, and diagnostic partners.
  • Represent BeOne Medicines at scientific meetings, external collaborations, and consortium activities.
  • Drive publication and presentation of high-impact translational and biomarker research in peer-reviewed journals and scientific congresses.

Desired Qualifications

  • Experience supporting companion diagnostic development is highly desirable.
  • Experience contributing to regulatory submissions involving biomarkers and precision medicine is preferred.
  • Knowledge of Mandarin is beneficial but not required.

About the Company

BeOne

Global oncology therapeutics discovery, development, manufacturing

BeOne Medicines discovers, develops, and commercializes oncology therapies worldwide, focusing on hematologic cancers and solid tumors. Its products work by leveraging internal R&D and clinical development to bring therapies to market quickly, with Brukinsa serving as a leading backbone in the US and European markets. It differentiates itself through a large-scale global clinical network and cost-efficient development and manufacturing that support high margins and a focus on large-market cancer indications. Its goal is to expand access to high-impact, affordable cancer treatments across more than 45 countries while growing its pipeline into immunology and solid tumors.

Company size
1,001-5,000
Company stage
IPO
Headquarters
Dongcheng District, China
Founded
2010

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