Senior Statistical Programmer/Analyst Consultant – CVRM, Cardiovascular, Renal & Metabolism

🕒 May 19

🇬🇧 United Kingdom – Remote

⏳ Contract/Temporary

🟠 Senior

🖥 Software Engineer

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ClinChoice

WebsiteLinkedInAll Job Openings

1001 - 5000 employees

Founded 1998

🧬 Biotechnology

💊 Pharmaceuticals

⚕️ Healthcare Insurance

Biotechnology • Pharmaceuticals • Healthcare Insurance

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

• The Senior Statistical Programmer Consultant is a delivery-focused role who works under the leadership, oversight, and direction of a Programming team leader to lead and/or support aspects of the programming effort to deliver technical programming and information components of a project. • 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 in 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 • Experience supporting regulatory submissions is preferred • Strong communication and stakeholder management skills.

🏖️ Benefits

• ClinChoice offers a strong focus on quality, professional development, and supportive culture.