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- Tasks: Lead statistical programming for clinical trials, ensuring data quality and submission readiness.
- Company: IQVIA is a global leader in clinical research and healthcare intelligence.
- Benefits: Enjoy remote work, great work/life balance, and career advancement opportunities.
- Why this job: Join a passionate team reshaping healthcare while working with top pharmaceutical companies.
- Qualifications: BSc in a relevant field and 5+ years of experience in statistical programming using SAS.
- Other info: Work in a collaborative environment across diverse therapeutic areas and study phases.
The predicted salary is between 48000 - 72000 £ per year.
Senior Statistical Programmer (Remote – Permanent Homebased)
IQVIA, Livingston, Scotland, United Kingdom
Posted 1 week ago
Why IQVIA
This role will be dedicated to one of IQVIA’s largest clients through a Functional Service Provider (FSP) type partnership. This means you get all the benefits of working for an industry leading global CRO while operating within a sponsor environment and utilizing sponsor systems. These sponsor clients include world class pharmaceutical and biotech companies offering you a unique opportunity to work on a team where your role is both challenging and rewarding, while working alongside colleagues who are passionate about influencing the future of medicine and advancing therapies. With IQVIA\’s FSP business unit, you become a core part of a dynamic team dedicated to reshaping the future of healthcare.
Additional 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
Job Description
The Senior Statistical Programmer will be responsible for review datasets in submission ready standard format (ADaM), tables, figures, listings and submission packages. This individual will provide expertise in the design, development and quality control process for SAS programs used to access, extract, transform, review, analyze and submit clinical data for all requested analyses.
Main Responsibilities And Accountabilities
- Collaborates with the study teams to design data structure and specifications for ad hoc and study deliverables including, but not limited to ADaM datasets, Tables, Figures, Listings and Analysis Submission content.
- Collaborates with study teams to ensure the quality and accuracy – thus submission readiness – of clinical data as required by authorities (i.e. SDTM, ADaM, tables, figures, listings, define.xml).
- Leads and oversees requested efforts for pooled and exploratory analyses working closely with Statistics TA lead and/or study statisticians as well as with clinical programming team and their collection of legacy data.
- Leads and oversees the in-house specification and delivery of ISS and ISE datasets and associated output (tables, figures and listings) when not provided by CRO.
- Leads and oversees the design and implementation of complex SAS programs for applications designed to analyze and report complex clinical trial data in CDISC ADaM format.
- Leads and oversees the development of global tools that will increase the efficiency and capacity of the Statistical Programming group.
- Works closely with clinical study teams to plan and execute activities to ensure project timelines are met with high quality deliverables.
Additional Tasks
- Collaborates with CR&D staff regarding data analysis requests.
- Performs additional statistical analyses including but not limited to:
- support responses to regulatory agencies
- generate integrated summary of safety and efficacy
- support publications and presentations
- support planning and reporting of clinical trials via exploratory analyses of available data
Position Qualifications And Experience Requirements
Education
- BSc in Computer Science, Mathematics, Statistics or related area with relevant experience
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.
- In-depth understanding of regulatory requirements relevant to statistical programming (e.g. GCP, ICH).
- Extensive experience with statistical programming using the SAS software including development and use of SAS Macros. Strong programming and problem-solving skills.
- 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.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com
- Seniority level: Mid‑Senior level
- Employment type: Full‑time
- Job function: Research, Analyst, and Information Technology
- Industry: Hospitals and Health Care
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Senior Statistical Programmer (Remote - Permanent Homebased) employer: IQVIA
Contact Detail:
IQVIA Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior Statistical Programmer (Remote - Permanent Homebased)
✨Tip Number 1
Familiarise yourself with the specific requirements of the Senior Statistical Programmer role. Make sure you understand the key responsibilities, such as working with ADaM datasets and SAS programming, so you can confidently discuss your relevant experience during interviews.
✨Tip Number 2
Network with professionals in the clinical programming field, especially those who work at IQVIA or similar companies. Engaging with them on platforms like LinkedIn can provide insights into the company culture and expectations, which can be invaluable during your application process.
✨Tip Number 3
Prepare to showcase your problem-solving skills and experience with SAS software. Be ready to discuss specific projects where you led programming activities or contributed to complex analyses, as this will demonstrate your capability to handle the challenges of the role.
✨Tip Number 4
Research IQVIA's recent projects and innovations in the pharmaceutical sector. Being knowledgeable about their work will not only help you tailor your application but also allow you to engage in meaningful conversations during interviews, showing your genuine interest in the company.
We think you need these skills to ace Senior Statistical Programmer (Remote - Permanent Homebased)
Some tips for your application 🫡
Tailor Your CV: Make sure to customise your CV to highlight relevant experience in statistical programming and clinical trials. Emphasise your proficiency with SAS software and any experience you have with CDISC standards.
Craft a Strong Cover Letter: Write a compelling cover letter that explains why you're interested in the Senior Statistical Programmer role at IQVIA. Mention specific projects or experiences that align with the responsibilities outlined in the job description.
Highlight Relevant Skills: In your application, clearly outline your skills in data analysis, programming, and project management. Provide examples of how you've successfully led programming activities or collaborated with cross-functional teams.
Proofread Your Application: Before submitting, carefully proofread your application for any spelling or grammatical errors. A polished application reflects your attention to detail, which is crucial for a role that involves data accuracy.
How to prepare for a job interview at IQVIA
✨Showcase Your Technical Skills
As a Senior Statistical Programmer, you'll need to demonstrate your expertise in SAS programming and statistical analysis. Be prepared to discuss specific projects where you've successfully implemented SAS solutions, and highlight your experience with CDISC standards.
✨Understand the Regulatory Landscape
Familiarise yourself with the regulatory requirements relevant to statistical programming, such as GCP and ICH guidelines. During the interview, be ready to explain how you ensure compliance in your work and how you handle data submission processes.
✨Emphasise Collaboration Experience
This role involves working closely with study teams and cross-functional groups. Share examples of how you've effectively collaborated with others in previous roles, particularly in a multicultural or international setting, to achieve project goals.
✨Prepare for Problem-Solving Questions
Expect questions that assess your problem-solving abilities, especially in relation to complex data analysis. Think of scenarios where you've encountered challenges in programming or data management, and be ready to discuss how you overcame them.