Remote Biostatistics Director – Clinical Programs

Jobgether; United States; Remote; USD 200,000 - 230,000; Full time

Benefits offered by this job

Comprehensive medical, dental, and vision coverage

Retirement plan with employer match

Paid Time Off and flexible leave policies

Professional development opportunities

Job summary

A biotech company is seeking an Associate Director / Director of Biostatistics to lead statistical strategy and execution for clinical development programs. The ideal candidate will have a PhD in Biostatistics and a strong background in clinical trials. This remote role offers a competitive salary of $200,000 to $230,000, comprehensive benefits, and the opportunity to mentor teams while contributing to regulatory submissions. Travel is limited to approximately 10%.

Qualifications

• 8+ years in industry for PhD or 11+ years for MS in drug development.
• Experience in pharmaceutical/biotech industry with statistical leadership.
• Strong background in clinical trial design and regulatory submissions.

Responsibilities

• Lead statistical strategy for clinical programs and trial design.
• Provide leadership on Study Executive Teams and ensure quality outputs.
• Contribute to regulatory submissions and interact with regulatory authorities.
• Oversee teams and ensure compliance of statistical deliverables.
• Interpret analysis results for reports and presentations.

Skills

Statistical leadership

Clinical trial design

Cross-functional collaboration

Regulatory submissions

CDISC standards

SAS

R

Analytical rigor

Education

PhD in Biostatistics or Statistics

MS with 11+ years in drug development

Job description

A biotech company is seeking an Associate Director / Director of Biostatistics to lead statistical strategy and execution for clinical development programs. The ideal candidate will have a PhD in Biostatistics and a strong background in clinical trials. This remote role offers a competitive salary of $200,000 to $230,000, comprehensive benefits, and the opportunity to mentor teams while contributing to regulatory submissions. Travel is limited to approximately 10%.