Senior Statistical Programmer - Consultant

3 days ago

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ClinChoice

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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.

Full-Service CRO • Clinical Development • Post-Marketing & Real-World Evidence • Quality and Compliance • Technology

1001 - 5000 employees

Founded 1998

🧬 Biotechnology

💊 Pharmaceuticals

⚕️ Healthcare Insurance

📋 Description

• Are you interested in working directly for a single sponsor while having the security and additional career opportunities that working for a global CRO can bring? Our team says it’s the best of both worlds... • ClinChoice is searching for a Senior Statistical Programmer Consultant to join one of our clients. • ClinChoice is a global full-service CRO with a strong focus on quality, professional development, and supportive culture. As a client-facing role, we are looking for confident candidates with the ability to work independently whilst establishing a high-trust environment with the client’s counterparts. • Main Job Tasks and 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 analyses of clinical trial data. • Responsible for 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. • Experience with CDISC data standards required. • Experience as a senior statistical programmer level in a pharmaceutical or CRO working in a 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.