Associate Director, Biostatistics

Associate Director, Biostatistics

If you are a Director, Biostatistics with 10+ years of clinical trial experience, please read on! 
Job Title: Associate Director, Biostatistics
Location: Cambridge, MA. MUST BE ON-SITE 5 DAYS A WEEK.
Salary: $135,000 - 200,000 + generous bonus & profit sharing.
Requirements: MUST HAVE EXPERIENCE WORKING DIRECTLY FOR A CRO (CLINICAL RESEARCH ORGANIZATION).  Master's degree in Biostatistics required.  PhD degree in Biostatistics preferred.  Minimum of 15 years of experience in clinical trials, including protocol design activities.  Minimum of 5 years of staff management experience required.  Knowledge of SAS statistical computing package is a must.

Position Overview
The Associate Director of Biostatistics will lead the statistical analysis and interpretation of clinical trial data. This role is critical in supporting the design, execution, and reporting of clinical studies, ensuring compliance with regulatory standards while delivering high-quality statistical insights to inform decision-making.

Key Responsibilities

• Lead statistical analysis and interpretation for clinical trials
• Develop and implement statistical methodologies and study designs
• Collaborate with cross-functional teams to ensure alignment of statistical strategies with clinical goals
• Manage and mentor a team of biostatisticians and data analysts
• Oversee data management processes to ensure data integrity and compliance
• Provide statistical input for regulatory submissions and documentation
• Utilize SAS, R, and other programming languages for data analysis and reporting
• Conduct statistical modeling and simulations to support research objectives
• Facilitate communication of results to stakeholders and present findings at scientific meetings

Qualifications

• Master's degree or PhD in Biostatistics, Statistics, or a related field
• 5+ years of experience in biostatistics within the pharmaceutical or biotechnology industry
• Strong knowledge of statistical analysis, clinical trials, and research methodology
• Proficiency in SAS, R, and data management tools
• Experience in regulatory submissions and compliance
• Demonstrated ability to manage projects and collaborate across functions
• Strong analytical skills and attention to detail
• Excellent communication and presentation skills

Benefits

• Medical, Dental, and Vision Insurance
• 401(k) Plan
• Paid Maternity/Paternity Leave
• Paid Vacation and Holidays
• Flexible Spending Accounts
• Disability and Life Insurance
• Tuition Reimbursement
• Flexible Work Schedule
• Employee Assistance Program
• Career Development Opportunities

For this position you must be currently authorized to work in the United States. We do not sponsor for this position.