Note: The job is a remote job and is open to candidates in USA. ClinChoice is a global full-service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies. They are searching for a Principal Statistical Programmer Consultant to work directly with a single sponsor, focusing on data management and analysis for clinical trials.
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
- 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
Company Overview
Company H1B Sponsorship