Senior Director of Statistical Programming & Data Strategy

Uniquity Design Group; San Diego (CA); On-site; USD 150,000 - 200,000; Full time

Job summary

Uniquity Design Group is seeking a Senior Director, Head of Statistical Programming to lead and enhance our statistical programming function. The role demands a candidate with a strong leadership background, deep technical expertise, and a thorough understanding of clinical trial processes.

Located in San Diego, CA, or Malvern, PA, this position involves direct collaboration with Biostatistics and Clinical Operations teams to ensure the highest quality of statistical outputs for regulatory submissions. Candidates must have significant experience within the biotech field and possess strong communication and organizational skills.

Qualifications

• Typically, 12+ years of statistical programming experience in biotechnology or CRO industry.
• Experience leading statistical programming activities across multiple phases of clinical development.
• Expertise in CDISC standards, including SDTM and ADaM implementation.

Responsibilities

• Define and lead the vision and operational strategy for the Statistical Programming function.
• Build and mentor statistical programming capabilities through strategic hiring and coaching.
• Oversee programming deliverables for clinical development programs.

Skills

SAS proficiency

Leadership

Statistical programming

CDISC standards

Collaboration

Education

Bachelor’s, Master’s, or PhD in Statistics, Biostatistics, Computer Science, Mathematics

Tools

SAS

R

Python

Job description

Uniquity Design Group is seeking a Senior Director, Head of Statistical Programming to lead and enhance our statistical programming function. The role demands a candidate with a strong leadership background, deep technical expertise, and a thorough understanding of clinical trial processes.

Located in San Diego, CA, or Malvern, PA, this position involves direct collaboration with Biostatistics and Clinical Operations teams to ensure the highest quality of statistical outputs for regulatory submissions. Candidates must have significant experience within the biotech field and possess strong communication and organizational skills.