Client-Facing Principal Statistical Programmer Consultant

ClinChoice; United States; On-site; USD 120,000 - 170,000; Full time

Job summary

ClinChoice is seeking a Principal Statistical Programmer Consultant to join one of our clients. This client-facing role requires independence and a high-trust relationship with the sponsor.

The candidate will contribute to data management, analysis, and reporting across studies within a project and collaborate with CROs and vendors. The position emphasizes extensive SAS programming expertise, CDISC data standards, and experience in FDA-regulated environments, with responsibilities including CRF

Qualifications

• Minimum of 10 years of SAS programming in the pharmaceutical or biotechnology industry with a BA/BS in computer science, statistics, math, or MA/MS with 8 years of experience.
• Expertise in SAS programming language, report generation, and standards for programming and validation.
• Therapeutic area- Rare Disease.
• Experience With CDISC Data Standards Required.

Responsibilities

• Participate in CRF design, database review, data management plan, data review, data validation procedures, and review of data listings.
• Produce data listings, summary tables, and graphics for interim and final analyses.
• Integrate data across studies within a project. Test, document, review, and validate all programs according to department guidelines.
• Coordinate data transfer and/or programming standards with CROs and vendors. Validate analysis datasets and TFLs from vendors.
• Collaborate with other Biometrics functions for all activities related to the analysis of clinical trial data.
• Responsible for the execution of ad-hoc requests, manuscripts, posters, and presentations.

Skills

SAS programming

CDISC data standards

FDA-regulated environment

Data management and validation

Education

BA/BS in computer science, statistics, math

MA/MS in relevant field

Tools

SAS

CDISC

Job description

ClinChoice is seeking a Principal Statistical Programmer Consultant to join one of our clients. This client-facing role requires independence and a high-trust relationship with the sponsor.

The candidate will contribute to data management, analysis, and reporting across studies within a project and collaborate with CROs and vendors. The position emphasizes extensive SAS programming expertise, CDISC data standards, and experience in FDA-regulated environments, with responsibilities including CRF