Associate Director, Biostatistics — Oncology Trials & Equity

BeOne Medicines Ltd.; United States; On-site; USD 163,000 - 213,000; Full time

Benefits offered by this job

Equity awards

Employee stock purchase plan

Comprehensive benefits

Job summary

BeOne Medicines Ltd. in the United States seeks an experienced statistician to support hematology studies, review data, and develop and implement the SAP for CSR and health authority submissions.

The role involves collaborating across cross-functional teams, designing analyses, writing reports, and contributing to manuscripts. Requires PhD in Statistics or related field with 5+ years, or a Master’s with 8 years in clinical drug development; SAS and/or R experience.

Qualifications

• PhD in Statistics or related field with 5+ years of experience, or a Master’s degree with 8 years of experience in clinical drug development.
• Experience with clinical trials and regulatory guidance.
• Oncology experience preferred but not required.
• Strong written and oral communication skills and ability to work in a team and independently.

Responsibilities

• Develops or assists development of study protocols and SAPs and determines appropriate statistical methodology for data analysis.
• Participates in database design meetings to ensure data quality and analysis requirements.
• Collaborates with statistical programming staff to ensure programs meet analysis requirements and regulatory guidelines.
• Analyzes data and interprets results from clinical trials to meet study objectives under supervision.
• Prepares oral and written reports to communicate results of clinical trials to the project team.

Skills

Analytical thinking

Data analysis

Team collaboration

Education

PhD in Statistics or related field

Master's degree in Statistics or related field

Tools

SAS

R

Job description

BeOne Medicines Ltd. in the United States seeks an experienced statistician to support hematology studies, review data, and develop and implement the SAP for CSR and health authority submissions.

The role involves collaborating across cross-functional teams, designing analyses, writing reports, and contributing to manuscripts. Requires PhD in Statistics or related field with 5+ years, or a Master’s with 8 years in clinical drug development; SAS and/or R experience.