Director, Biostatistics — Lead Oncology Trials & Analytics

Celcuity Inc.; Northern (KY); Hybrid; USD 195,000 - 215,000; Full time

Benefits offered by this job

Annual incentive bonus

Equity package

Medical, dental, vision insurance

401(k) match

PTO and paid holidays

Job summary

Celcuity Inc. is seeking a Director of Biostatistics to lead statistical activities across multiple oncology studies. You will oversee statistical programming, write methods and analysis descriptions, and communicate results with collaborators while maintaining confidential materials.

Ideal candidates have a PhD (preferred) with 7+ years in clinical trials, including 2+ years in oncology. Expect collaboration across global submissions and a competitive compensation package.

Qualifications

• Master's degree in statistics/biostatistics; PhD preferred.
• 7+ years clinical trials experience, at least 2 years in oncology.
• Solid tumor oncology experience and NDA/BLA submissions preferred.
• Experience with design, execution, and reporting phase 3 oncology trials as lead statistician preferred.
• Strong knowledge of SAS and R; SQL scripting is a plus.

Responsibilities

• Lead and coordinate statistical activities to support clinical studies, including design, execution, analysis and reporting.
• Provide input to program plans and represent Biostatistics in cross-functional teams.
• Prepare or review protocols, CRFs, SAPs, and table shells.
• Create or validate SAS programs for data management and analysis.
• Prepare statistical sections of reports and present results to team.
• Oversight of CROs on statistical deliverables.
• Maintain confidential project materials.

Skills

Statistical programming

Strong writing

Prioritization

Communication

Education

Master's degree in statistics/biostatistics

PhD preferred

Tools

SAS

R

S-Plus

SQL

Job description

Celcuity Inc. is seeking a Director of Biostatistics to lead statistical activities across multiple oncology studies. You will oversee statistical programming, write methods and analysis descriptions, and communicate results with collaborators while maintaining confidential materials.

Ideal candidates have a PhD (preferred) with 7+ years in clinical trials, including 2+ years in oncology. Expect collaboration across global submissions and a competitive compensation package.