
Associate Director, Clinical Biomarker
Emeryville, CAJobSeen 4w agoSeen in employer's feed 3 days ago
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Job overview
BeOne Medicines seeks an Associate Director of Clinical Biomarker & Translational Medicine to lead global biomarker strategy for solid tumor oncology, overseeing assay development, validation, data analysis, and regulatory submissions while collaborating with cross‑functional teams and external partners to accelerate clinical trials and pipeline advancement.
Skills & qualifications
Skills
Qualifications
Full job description
General Description:
We are seeking an Associate Director of Clinical Biomarker & Translational Medicine for Oncology (Solid Tumor Portfolio, GI franchise) to provide strategic, scientific, and operational leadership across our clinical biomarker initiatives for solid tumor oncology programs. This role is pivotal in driving the development and execution of innovative biomarker strategies that accelerate our clinical trials and pipeline advancement.
Essential Functions of the Job:
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Lead global clinical biomarker strategy for solid tumor oncology, in partnership with cross-functional teams, ensuring effective design and implementation of biomarker and companion diagnostic initiatives throughout the drug development continuum.
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Oversee biomarker assay development and validation, including scientific input on assay design, proficiency testing, and analytical/clinical validation, ensuring readiness for regulatory and clinical decision points.
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Direct the comprehensive analysis and interpretation of biomarker data to inform go/no-go decisions and trial advancement.
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Effectively communicate with internal and external stakeholders, translating biomarker data into tangible insights and strategy recommendations.
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Serve as scientific leader and subject matter expert, actively contributing to scientific discussions, program strategy, and the advancement of clinical stage projects.
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Drive and manage external partnerships with academic institutions, CROs, and industry partners to enhance biomarker discovery and development efforts.
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Contribute to regulatory submissions related to biomarker strategies and companion diagnostics.
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Champion biomarker-related publications, driving thought leadership and innovation in oncology drug development.
Supervisory Responsibilities:
- Not required
Requirements :
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PhD or MD/PhD in a relevant scientific discipline, with 5+ years’ experience in pharmaceutical or biotechnology settings, focusing on biomarker science in oncology.
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Deep expertise in biomarker discovery, clinical assay development, and validation (including proficiency in designing and analyzing biomarker-driven clinical trials). Strong experience in pe-clinical oncology research and drug discovery.
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Demonstrated leadership in translational medicine, with a track record of successful biomarker strategies leading to regulatory submissions, approvals, or high-impact publications.
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Experience managing cross-functional and cross-institutional teams.
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Excellent communication, reporting, and presentation skills.
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Proven ability to thrive in dynamic, fast-paced environments and to mentor junior scientists and project teams.
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Strong publication record and/or regulatory contributions in oncology clinical development.
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Mandarin language proficiency is required.
Travel:
- Not required
Education Required:
PhD or MD/PhD in a relevant scientific discipline.
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
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