Senior Statistical Programmer/Analyst Consultant – Oncology

🔥 12 hours 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%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

Apply Now

Find Similar Remote Jobs

Set Up Email Alert For New Jobs

📊 Check your resume score for this job

Improve your chances of getting an interview by checking your resume score before you apply.

Upload Resume

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 of a clinical study or project • Implement statistical programming aspects of protocols and clinical development programs • Ensure high quality in own deliverables and work delivered by other programmers • Program independently with high efficiency and quality • Write and/or implement specifications and oversee completeness of relevant documentation • 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 and/or projects • Work proactively with Statisticians, Lead Programmers, Data Managers, Study Leaders, and other study team members • Work under the leadership, oversight, and direction of a Programming team leader

🎯 Requirements

• Bachelor’s degree in computer science (CS), statistics, or related scientific disciplines with 5 yrs. of clinical programming (CDISC) experience, or Master’s degree in CS, statistics or related disciplines with 6 yrs. of clinical programming (CDISC) experience • Oncology TA experience • Working knowledge of ICH and Good Clinical Practices, clinical research, clinical trial process, 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 for the role • Ability to proactively manage concurrent activities within a project • Proficient ability to influence relevant stakeholders on programming-related items

🏖️ Benefits

• Security and additional career opportunities from working for a global CRO • Professional development • Supportive culture • Continuous training • Close management and training • Equal opportunity and diversity and inclusivity