Senior Statistical Programmer/Analyst Consultant – Oncology

🔥 13 hours ago

🇺🇸 United States – Remote

⏳ Contract/Temporary

🟠 Senior

🖥 Software Engineer

🦅 H1B Visa Sponsor

This company has sponsored H1B visas in the past.

👻 Ghost score 10%

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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

• Support programming deliveries for a clinical study or project • Implement statistical programming aspects of protocols and clinical development programs • Ensure high quality in personal and other programmers’ deliverables • Program independently with high efficiency and quality • Write or implement specifications and oversee relevant documentation completeness • Contribute to best practices improving quality, efficiency, and effectiveness • Ensure compliance with standards and automation usage • Plan and support team activities and tasks • Communicate and escalate risks within assigned studies or projects • Work proactively with Statisticians, Lead Programmers, Data Managers, and Study Leaders

🎯 Requirements

• Bachelor’s degree in computer science, statistics, or related scientific disciplines with 5 years of clinical programming (CDISC) experience, or Master’s degree in CS, statistics, or related disciplines with 6 years of clinical programming (CDISC) experience • Oncology therapeutic area experience • Working knowledge of ICH and Good Clinical Practices, clinical research, clinical trial processes, and related regulatory requirements and terminology • Good understanding of the clinical drug development process • Strong communication and coordination skills • Current knowledge of technical and regulatory requirements relevant to the role • Ability to proactively manage concurrent project activities • Ability to influence relevant stakeholders on programming-related items

🏖️ Benefits

• Professional development and continuous training • Supportive culture • Close management and training • Career opportunities through a global CRO • Equal opportunity and diversity-focused workplace