Senior Clinical Scientist – Oncology

Key Responsibilities

• Lead the development and execution of Clinical Development Plans (CDP), including strategy, indication prioritization, and milestone planning
• Provide scientific input into protocol design, study endpoints, and data analysis plans for Phase III oncology studies
• Serve as the scientific lead on cross-functional study teams
• Author and review key documents including protocols, investigator brochures, clinical study reports, and regulatory submissions (INDs, CTAs)
• Partner with Clinical Operations to support study execution, data review, and issue resolution
• Collaborate with Biostatistics on statistical analysis plans and endpoint development
• Engage with Key Opinion Leaders (KOLs) and support investigator meetings and external collaborations
• Represent Clinical Science in governance and cross-functional discussions

Required Qualifications

• Ph.D. or PharmD with 10+ years of industry experience
• Strong background in oncology clinical development
• Experience leading or contributing to global Phase III clinical trials
• Deep understanding of oncology biology, translational science, and PK/PD
• Proven experience developing and executing Clinical Development Plans
• Excellent scientific writing, data interpretation, and communication skills

Benefits

Remote work with PST working hours preferred

Pay

TBD

Schedule

Initial 3 months with potential extension