Principal Statistical Programmer/Analyst Consultant

🔥 1 hour ago

🇺🇸 United States – Remote

⏰ Full Time

🔴 Lead

🖥 Software Engineer

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ClinChoice

WebsiteLinkedInAll Job Openings

1001 - 5000 employees

Founded 1998

💼 Consulting

🏥 Healthcare

📦 Logistics

Consulting • Healthcare • Logistics

ClinChoice is a global full-service contract research organization (CRO) established in 1995, specializing in clinical development, post-marketing, and functional service support for the pharmaceutical, biotechnology, and medical devices industries. They provide comprehensive solutions from early clinical development to post-approval lifecycle management, with expertise in a variety of therapeutic areas such as autoimmune and inflammation, dermatology, endocrinology, infectious diseases, neuroscience, and oncology. ClinChoice aims to contribute to a healthier and safer world by accelerating the development and commercialization of innovative drugs and devices. The company supports its clients with clinical, regulatory, and operational expertise across all phases of product development.

📋 Description

• 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.

🎯 Requirements

• 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.

🏖️ Benefits

• ClinChoice offers a supportive culture • Professional development opportunities