Director, Biostatistics (Oncology) - FILLED

North Davis Executive Search; United States; Remote; USD 150,000 - 200,000; Full time

Job summary

An established industry player is seeking a Director of Biostatistics to lead Biometrics and Data Integrity efforts. This pivotal role will involve overseeing statistical work in clinical development, HEOR/RWE, and medical affairs studies, ensuring high-quality data analysis and statistical planning, particularly in oncology diagnostics and therapeutics. The ideal candidate will have extensive experience in trial design and a solid understanding of clinical programming. This fulltime, permanent position offers the flexibility to work from anywhere in the U.S., making it a fantastic opportunity for professionals looking to make a significant impact in the field.

Qualifications

• Proven experience in statistical planning and data analysis in oncology.
• Hands-on experience with trial design and EDC data capture.

Responsibilities

• Oversee statistical work across clinical development and medical affairs studies.
• Guide external vendors in biostatistics and clinical programming.

Skills

Statistical Planning

Data Analysis

Trial Design

EDC Data Design

Clinical Programming

Data Management

Job description

The Director of Biostatistics will report to the CMO and will be the head of Biometrics and Data Integrity. The position will oversee and guide the statistical work across early and late phase clinical development, HEOR/RWE and medical affairs studies which includes biostatistics and clinical programming work performed by external vendors.

The successful candidate will need to have proven experience in statistical planning and data analysis in oncology diagnostic and therapeutic development, ideally in nuclear medicine and radio-ligand field. The candidate will have a comprehensive understanding of and hands-on experience with trial design, EDC data design and capture, Statistical Analysis Plans (SAP), providing guidance on Table, Listing and Figures, conducting data analysis and data exploration as well as a working knowledge of clinical programming and data management.

This is a fulltime, permanent position with a sponsor company and can be based anywhere in the U.S.