Director, Clinical Sciences

• Scientific contribution to one or more clinical programs to ensure the successful design, execution, and interpretation of clinical studies
• Provide scientific leadership throughout the design, execution, analysis, and interpretation of early- and late-stage oncology clinical trials
• Partner closely with Clinical Development physicians, Clinical Operations, Biostatistics, Clinical Pharmacology, Pharmacovigilance, Regulatory Affairs, Translational Medicine, and Medical Writing to ensure high-quality execution of clinical programs
• Contribute to the development and review of key clinical documents, including protocols, investigator brochures, informed consent forms, clinical study reports, clinical development plans, and regulatory briefing materials
• Interpret emerging clinical, safety, PK/PD, and biomarker data to inform study conduct, dose selection, expansion opportunities, and overall development strategy
• Contribute scientific expertise to regulatory submissions and health authority interactions
• Foster a collaborative, accountable, and scientifically rigorous culture within the Clinical Science function
• Perform additional duties and responsibilities as required

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