Lead Statistical Programmer – Clinical Trials

Connect Life Sciences; United States; On-site; USD 120,000 - 160,000; Full time

Job summary

Connect Life Sciences is seeking an experienced Statistical Programmer with leadership responsibilities to design and oversee analysis data models for clinical trials. You will develop SAS programs, validate outputs, and ensure quality across multi-trial datasets, including SDTM/ADaM mappings.

The role requires a North American degree and 8+ years in statistical programming, with the ability to guide junior staff and liaise with sponsors.

Qualifications

• Master’s degree in Statistics, Biostatistics, Computer Science, or a related field.
• 8+ years of experience in statistical programming or biostatistics.
• Must have a degree from North America.

Responsibilities

• Lead complex statistical programming projects, coordinating study teams and timelines.
• Provide mentorship and technical guidance to junior programmers.
• Perform hands-on SAS programming, validation, and QC of deliverables.
• Develop SDTM/ADaM specifications and define.xml files with QC reviews.
• Ensure adherence to regulatory standards and corporate SOPs.

Skills

Leadership

Project management

Mentorship

Communication

Education

Master’s degree in Statistics/Math/CS

Tools

SAS

CDISC standards

Job description

Connect Life Sciences is seeking an experienced Statistical Programmer with leadership responsibilities to design and oversee analysis data models for clinical trials. You will develop SAS programs, validate outputs, and ensure quality across multi-trial datasets, including SDTM/ADaM mappings.

The role requires a North American degree and 8+ years in statistical programming, with the ability to guide junior staff and liaise with sponsors.