Principal Programmer

What you'll do

• Lead programming activities and develop, maintain, and validate complex analysis packages for one or more studies.
• Ensure quality and compliance with Good Programming Practices, CDISC standards, and regulatory requirements; identify risks and implement improvements.
• Mentor junior programmers and lead programming support for regulatory interactions such as EMA and FDA.

What they ask for

• 5+ years of programming experience in pharmaceutical, biotechnology, healthcare, or another regulated industry.
• Programming experience with one or more languages such as SAS, R, Python, or a comparable language.
• Experience supporting clinical trials, clinical development programs, or analysis of clinical research data, including developing, validating, and maintaining custom programs or analyses.
• Experience applying programming standards, quality control procedures, and regulatory requirements in a regulated environment; expertise in oncology requirements such as RECIST1.1.

Nice to have

• Experience guiding others in using AI/ML tools or applying them to improve efficiency.
• Strong expertise in CDISC standards and demonstrated proficiency in R.

Pay

$126,225 to $210,375 USD annual base salary; annual bonus and share-based long-term incentive eligibility are also offered, with no amounts stated.

Tools

SAS, R, Python, CDISC, RECIST1.1, AI/ML

AI focus

Preferred experience includes guiding others in using AI/ML tools or applying them to improve efficiency.