Principal Statistical Programmer

BioSpace; Basking Ridge (NJ); On-site; USD 108,000 - 177,000; Full time

Job summary

A forward-thinking company seeks a Principal Statistical Programmer to lead programming efforts in clinical trials. This pivotal role involves developing analysis datasets, validating plans, and collaborating with multidisciplinary teams to ensure high-quality data processing. With a focus on innovation and efficiency, you'll support various departments and enhance tools and processes. This full-time position offers a competitive salary and comprehensive benefits, fostering an inclusive culture that values diversity and supports employee well-being. If you're passionate about making a difference in the biotech and pharma industries, this opportunity is for you.

Benefits

Health programs

Fitness centers

Bonuses

Paid time off

Qualifications

• 3+ years of programming experience in clinical trial data.
• Proficiency in SAS for data analysis and reporting.

Responsibilities

• Lead programming and QC of analysis datasets and TFLs.
• Create and maintain programming specifications for datasets.
• Collaborate with teams for clinical trial analysis.

Skills

SAS (Base, Stat, Macro, Graph)

Programming in clinical trial data

Statistical analysis

Education

Master's Degree in Statistics

Master's Degree in Computer Science

Master's Degree in Mathematics

Master's Degree in Engineering

Master's Degree in Life Science

Job description

Join us as a Principal Statistical Programmer at BioSpace

We are seeking a Principal Statistical Programmer to provide timely support to study teams on all programming matters, according to project strategies. This role involves project leadership and programming support for processing data from clinical studies, with responsibilities including development of analysis datasets, validation plans, and documentation in a regulated environment.

Key Responsibilities:

1. Support and lead programming and QC of analysis datasets, TFLs, or standard tools following company standards.
2. Coordinate activities and communicate timelines and milestones.
3. Integrate data across studies to support various departments.
4. Create and maintain programming specifications for analysis datasets.
5. Support creation and validation of submission documents.
6. Collaborate with multidisciplinary teams to support clinical trial analysis and reporting.
7. Develop and deliver training on applications and tools.
8. Support basic statistical ad-hoc requests and data presentations.
9. Participate in departmental working groups to improve tools and processes.

Minimum Requirements:

• Master's Degree in Statistics, Computer Science, Mathematics, Engineering, Life Science, or related field.
• 3+ years of programming experience in processing clinical trial data, preferably in biotech, pharma, or health industries.
• Proficiency in SAS (Base, Stat, Macro, Graph).

This position offers a salary range of $108,300 to $176,700 annually, and is classified as a Mid-Senior level, full-time role within the Research, Analyst, and Information Technology fields.

Regeneron promotes an inclusive culture with comprehensive benefits, including health programs, fitness centers, bonuses, and paid time off. We are an Equal Opportunity Employer committed to diversity and accommodation for applicants with disabilities.