Associate Director, Clinical Biomarker

This is a fully remote position, open to applicants in United States.

📋 Description

• Lead the global clinical biomarker strategy for solid tumor oncology in collaboration with cross-functional teams.

• Design and execute biomarker and companion diagnostic initiatives throughout the drug development process.

• Supervise the development and validation of biomarker assays, encompassing assay design, proficiency testing, and analytical/clinical validation.

• Direct the analysis and interpretation of biomarker data to guide go/no-go decisions and the advancement of trials.

• Engage with internal and external stakeholders, translating biomarker data into strategic recommendations.

• Act as the scientific leader and subject matter expert in scientific discussions, program strategies, and clinical-stage projects.

• Manage collaborations with academic institutions, CROs, and industry partners.

• Contribute to regulatory submissions concerning biomarker strategies and companion diagnostics.

• Advocate for biomarker-related publications and thought leadership in the field of oncology drug development.

⛳️ Requirements

• PhD or MD/PhD in a relevant scientific field.

• Over 5 years of experience in pharmaceutical or biotechnology environments, with a focus on biomarker science in oncology.

• Extensive expertise in biomarker discovery, development of clinical assays, and validation processes.

• Experience in designing and analyzing biomarker-driven clinical trials.

• Strong background in pre-clinical oncology research and drug discovery.

• Proven leadership in the field of translational medicine.

• A history of successful biomarker strategies that have led to regulatory submissions, approvals, or impactful publications.

• Experience managing cross-functional and cross-institutional teams.

• Excellent skills in communication, reporting, and presentations.

• Capability to excel in dynamic, fast-paced environments.

• Ability to mentor junior scientists and project teams.

• Strong publication record and/or contributions to regulatory affairs in oncology clinical development.

• Proficiency in Mandarin is required.

🏝️ Benefits

• Eligibility for an annual bonus plan for Non-Commercial roles.

• Eligibility for an incentive compensation plan for Commercial roles.

• Discretionary equity awards.

• Employee Stock Purchase Plan.

• Medical insurance.

• Dental insurance.

• Vision insurance.

• 401(k) plan.

• Flexible Spending Account (FSA) / Health Savings Account (HSA).

• Life insurance.

• Paid Time Off.

• Wellness programs.