Principal Statistical Programmer

Scorpion Therapeutics; Boston (MA); Hybrid; USD 150,000 - 210,000; Full time

Job summary

Scorpion Therapeutics seeks a Principal Statistical Programmer to lead clinical trial data analysis and submission activities. You will manage SAS programming, ensure data quality, and support regulatory deliverables for development programs.

You will collaborate with Biostatistics, Data Management, and Regulatory Affairs across remote, hybrid, or onsite work setups, with flexible scheduling and no travel required.

Qualifications

• Bachelor’s degree in a scientific field and 8+ years in biotech/pharma/clinical research.
• Expertise in SAS programming and CDISC standards for regulatory submissions.
• Experience supporting eCTD submissions and regulatory deliverables.

Responsibilities

• Lead SAS programming for clinical trials and submission activities.
• Perform quality control and support regulatory submissions (eCTD, ISS/ISE).
• Collaborate with Biostatistics, Data Management, and Regulatory Affairs.

Skills

SAS programming

CDISC standards

Regulatory submissions

Education

Bachelor's degree in a scientific discipline

Tools

SAS

Job description

Role:

Principal Statistical Programmer leading clinical trial data analysis and submission activities.

Objectives include ensuring quality, compliance, and timely delivery of statistical outputs for clinical development programs.

Responsibilities:

Responsibilities cover SAS programming, quality control, supporting regulatory submissions (eCTD, ISS/ISE), and collaborating with cross-functional teams like Biostatistics, Data Management, and Regulatory Affairs.

Requirements:

Bachelor's in a Scientific discipline; 8+ years in biotech/pharma/clinical research with expertise in SAS, CDISC standards, and regulatory submissions.

Preferred:

advanced knowledge of clinical trial processes and regulatory standards.

HighValue:

extensive SAS proficiency, regulatory submission experience, validation of electronic data submissions, and compliance with FDA/ICH/GCP.

Work setup:

remote, hybrid, or onsite option with flexibility; no travel specified.