Lead Statistical Programmer – SAS & CDISC Expert

Vertex Pharmaceuticals Inc (US); United States; Remote; USD 137,000 - 205,000; Full time

Benefits offered by this job

Annual bonus

Equity awards

Remote-friendly

Job summary

Vertex Pharmaceuticals Inc (US) is seeking a Principal Statistical Programmer to lead statistical programming activities for clinical trials. The role involves leveraging SAS expertise, overseeing code quality, and guiding submission-ready analyses in collaboration with cross-functional teams.

The position supports eCTD data delivery, adheres to FDA/ICH/GCP regulations, and offers remote eligibility with flexible work arrangements.

Qualifications

• Proficiency in SAS language, procedures, and functions used in clinical trial reporting.
• CDISC standards knowledge.
• Experience with regulatory submission processes.

Responsibilities

• Delegate tasks, track progress, and provide expert technical support.
• Perform QA of SAS code and outputs for accuracy and consistency.
• Lead data analysis, reporting, and CDISC data submission support.
• Collaborate with cross-functional teams and senior management.

Skills

SAS language

SAS procedures

SAS/STAT

SAS/GRAPH

CDISC standards

Clinical trials

Regulatory submissions

Communication skills

Education

Bachelor's degree

MS or PhD preferred

Tools

eCTD

Job description

Vertex Pharmaceuticals Inc (US) is seeking a Principal Statistical Programmer to lead statistical programming activities for clinical trials. The role involves leveraging SAS expertise, overseeing code quality, and guiding submission-ready analyses in collaboration with cross-functional teams.

The position supports eCTD data delivery, adheres to FDA/ICH/GCP regulations, and offers remote eligibility with flexible work arrangements.