Senior Statistical Programmer Consultant (Remote)

ClinChoice; United States; Remote; USD 120,000 - 160,000; Full time

Benefits offered by this job

Remote work

Job summary

ClinChoice is seeking a Principal Statistical Programmer Consultant to join a client as a remote senior contributor. The role focuses on CRF design, data management, and validation for NDA submissions within an FDA-regulated setting.

Applicants should have extensive SAS expertise, CDISC standards experience, and a track record of delivering interim/final analyses while coordinating with CROs and vendors. Strong cross-functional collaboration is essential.

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.
• Experience as a senior statistical programmer at a pharmaceutical or CRO working in an FDA-regulated environment.
• Experience with Clinical Study Reports and NDA submission.
• Ability to work on multiple tasks simultaneously and meet project deadlines.
• Excellent verbal/written and interpersonal skills required for working successfully in a cross-functional team environment.

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

Data management

CDISC data standards

FDA-regulated environment

Interpersonal skills

Education

Bachelor's degree in computer science, statistics, math, or MA/MS

Tools

SAS

Job description

ClinChoice is seeking a Principal Statistical Programmer Consultant to join a client as a remote senior contributor. The role focuses on CRF design, data management, and validation for NDA submissions within an FDA-regulated setting.

Applicants should have extensive SAS expertise, CDISC standards experience, and a track record of delivering interim/final analyses while coordinating with CROs and vendors. Strong cross-functional collaboration is essential.