Principal Statistical Programmer - Late Phase, Cardiovascular, Renal, and Metabolism

February 26

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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? • ClinChoice is a global full-service CRO with a strong focus on quality, professional development, and supportive culture. • We are seeking a Principal Statistical Programmer to join our growing team in Late Phase Clinical - Cardiovascular, Renal, and Metabolism (CVRM). • This is a leadership role responsible for the strategic direction and delivery of programming activities across complex clinical development programs. • As a subject matter expert, you will guide teams in the implementation of statistical programming and provide technical leadership across a range of drug development projects. • You will be expected to lead the full scope of programming activities, ensuring the highest quality deliverables and efficient project delivery, while driving continuous improvement within the programming discipline.

🎯 Requirements

• Bachelor’s degree in Computer Science (CS), Statistics, Mathematics, or related scientific field. • 8+ years of SAS programming experience, with 4+ years of experience in Cardiovascular, Renal, and Metabolism (CVRM) clinical trials. • In-depth experience with CDISC standards (SDTM, ADaM) and an understanding of their application in clinical trials. • Working knowledge of ICH and Good Clinical Practices (GCP), clinical research processes, and related regulatory requirements. • Strong understanding of the clinical drug development process and experience with late-phase studies. • Excellent communication and coordination skills, with the ability to interact with global teams and stakeholders independently. • Proficient in risk management for complex or novel situations, demonstrating the ability to proactively address challenges. • Proven ability to influence relevant stakeholders, ensuring effective decision-making on programming-related matters. • Experience with programming leadership in cross-functional teams, driving project success and providing mentorship to junior staff.