Senior/Principal Statistical Programmer/Analyst Consultant – Cardiovascular, Renal

🔥 0 minutes ago

🇬🇧 United Kingdom – Remote

⏳ Contract/Temporary

🟠 Senior

🖥 Software Engineer

🇬🇧 UK Skilled Worker Visa Sponsor

This company has sponsored UK Skilled Worker 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

• Lead and/or support programming efforts under the leadership, oversight, and direction of a Programming team leader • Develop, validate, and maintain SAS programs for clinical study data analysis and reporting • Create datasets, tables, listings, and figures according to study requirements • Collaborate with Biostatistics, Data Management, and Clinical teams • Ensure programming deliverables meet quality standards and project timelines • Participate in study planning, review specifications, and support submission activities

🎯 Requirements

• Strong SAS programming experience within the pharmaceutical/CRO industry • Hands-on experience supporting CVRM (Cardiovascular, Renal & Metabolism) studies • Experience generating and validating SDTM, ADaM, and TLFs • Good understanding of CDISC standards and clinical trial processes • Ability to work independently and manage multiple priorities in a fast-paced environment • Strong communication and stakeholder management skills • 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 • Respiratory/Immunology therapeutic-area experience • Working knowledge of ICH, Good Clinical Practices, clinical research, clinical trial processes, regulatory requirements, and terminology • Experience supporting regulatory submissions is preferred

🏖️ Benefits

• Global CRO environment with security and additional career opportunities • Professional development and continuous training • Supportive culture • Close management and training • Equal opportunity and diversity-focused workplace