Senior Statistical Programmer – Permanent Homebased

🕒 July 14

🌐 United Kingdom, France, +12 more countries – Remote

🇬🇧 United Kingdom – Remote 🇫🇷 France – Remote 🇪🇸 Spain – Remote 🇺🇦 Ukraine – Remote 🇳🇱 Netherlands – Remote 🇮🇪 Ireland – Remote 🇩🇪 Germany – Remote 🇸🇮 Slovenia – Remote 🇷🇴 Romania – Remote 🇧🇪 Belgium – Remote 🇸🇪 Sweden – Remote 🇫🇮 Finland – Remote 🇸🇰 Slovakia – Remote 🇩🇰 Denmark – Remote

⏰ Full Time

🟠 Senior

🖥 Software Engineer

🇬🇧 UK Skilled Worker Visa Sponsor

This company has sponsored UK Skilled Worker visas in the past.

👻 Ghost score 55%

What it means: the chance that no one is really hiring for this job.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.Why this score:

• Open for 122 days.
• Jobs at this company usually fill in 24 days.
• Reposted once.
• No salary listed.

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IQVIA

WebsiteLinkedInAll Job Openings

10,000+ employees

💼 Consulting

🏭 Manufacturing

📣 Marketing

💰 $1G Post-IPO Debt on 2023-05

Consulting • Manufacturing • Marketing

IQVIA is a global leader in data analytics and technology solutions, dedicated to improving health outcomes. The company utilizes its Connected Intelligence platform to harness the power of advanced data analytics and artificial intelligence, facilitating innovation in healthcare. IQVIA focuses on various areas, including clinical research, technology, and consulting services to solve complex healthcare challenges and accelerate the delivery of new therapies to patients.

📋 Description

• Review datasets in submission-ready standard format (ADaM), tables, figures, listings and submission packages • Provide expertise in designing, developing and quality controlling SAS programs for accessing, extracting, transforming, reviewing, analyzing and submitting clinical data • Collaborate with study teams to design data structures and specifications for ad hoc and study deliverables, including ADaM datasets, tables, figures, listings and analysis submission content • Ensure the quality, accuracy and submission readiness of clinical data, including SDTM, ADaM, tables, figures, listings and define.xml • Lead and oversee pooled and exploratory analyses with Statistics TA leads, study statisticians, clinical programmers and legacy data teams • Lead and oversee in-house specification and delivery of ISS and ISE datasets and associated tables, figures and listings when not provided by CRO • Lead and oversee complex SAS programs for analyzing and reporting clinical trial data in CDISC ADaM format • Lead and oversee development of global tools to increase Statistical Programming group efficiency and capacity • Plan and execute activities with clinical study teams to meet project timelines and deliver high-quality outputs • Collaborate with CR&D staff regarding data analysis requests • Perform additional statistical analyses to support regulatory responses, integrated summaries of safety and efficacy, publications, presentations, and clinical trial planning and reporting

🎯 Requirements

• BSc in Computer Science, Mathematics, Statistics or related area with relevant experience • At least 5+ years of experience in either clinical programming and/or statistical programming, within the CRO/pharmaceutical environment using SAS Software • In-depth understanding of clinical programming and/or statistical programming processes and standards • Extensive experience with statistical programming using the SAS software including development and use of SAS Macros • Strong programming and problem-solving skills • Good experience in R Programming (Trained/Hands on experience) • Advanced knowledge in CDISC standards (CDASH, SDTM, ADaM) • Proven experience in leading programming activities for pooled and exploratory analyses across multiple clinical studies and submission activities (or equivalent) • Proven ability to work effectively both independently or in a team setting, and to meet set goals by managing own timelines • Experience in working in cross-functional, multicultural and international clinical trial teams

🏖️ Benefits

• Home-based remote work opportunities • Great work/life balance • Collaborate on projects and innovations with industry leaders in the Pharma and CRO sectors • Cohesive team environment fostering a collaborative approach to study work • Variety of therapeutic areas, indications and, study phases • Job stability; long-term engagements and development opportunities • Career advancement opportunities

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