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- Tasks: Lead the design and quality control of clinical data analysis using SAS programming.
- Company: Join IQVIA, a global leader in clinical research and healthcare intelligence.
- Benefits: Enjoy flexible working options and opportunities for professional growth.
- Why this job: Make a real impact on patient outcomes while collaborating with diverse teams.
- Qualifications: BSc in a relevant field with 5+ years of experience in statistical programming.
- Other info: Work in a multicultural environment with a focus on innovation and excellence.
The predicted salary is between 42000 - 84000 £ per year.
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Associate Principal Statistical Programmer (m/w/d), Reading
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Client:
IQVIA
Location:
Reading, United Kingdom
Job Category:
Other
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EU work permit required:
Yes
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Job Reference:
18c4a66eed36
Job Views:
5
Posted:
12.08.2025
Expiry Date:
26.09.2025
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Job Description:
The Associate Principal 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 plans and executes activities to ensure project timelines are met with high quality deliverables.
• Collaborates with CR&D staff regarding data analysis requests.
• Performs additional statistical analyses including but not limited to:
o support responses to regulatory agencies,
o generate integrated summary of safety and efficacy,
o support publications and presentations,
o 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.
• Indepth understanding of clinical programming and/or statistical programming processes and standards.
• Indepth 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
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Associate Principal Statistical Programmer (m/w/d) employer: IQVIA
Contact Detail:
IQVIA Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Associate Principal Statistical Programmer (m/w/d)
✨Tip Number 1
Familiarise yourself with the latest CDISC standards, especially ADaM, SDTM, and CDASH. This knowledge will not only help you understand the requirements of the role but also demonstrate your commitment to staying updated in the field.
✨Tip Number 2
Network with professionals in the clinical programming and statistical programming fields. Attend relevant conferences or webinars where you can meet people from IQVIA or similar companies, as personal connections can often lead to job opportunities.
✨Tip Number 3
Brush up on your SAS programming skills, particularly in developing and using SAS Macros. Consider working on sample projects or contributing to open-source projects to showcase your programming capabilities.
✨Tip Number 4
Prepare for potential interviews by reviewing common questions related to clinical data analysis and programming. Be ready to discuss your previous experiences leading programming activities and how you ensured quality and accuracy in your work.
We think you need these skills to ace Associate Principal Statistical Programmer (m/w/d)
Some tips for your application 🫡
Understand the Role: Before applying, make sure to thoroughly read the job description for the Associate Principal Statistical Programmer position. Understand the key responsibilities and qualifications required, as this will help you tailor your application.
Tailor Your CV: Customise your CV to highlight relevant experience in clinical programming and statistical programming, particularly with SAS software. Emphasise your understanding of CDISC standards and any leadership roles you've held in previous projects.
Craft a Compelling Cover Letter: Write a cover letter that connects your skills and experiences directly to the job requirements. Mention specific projects where you demonstrated your expertise in SAS programming and your ability to collaborate with study teams.
Proofread Your Application: Before submitting, carefully proofread your CV and cover letter for any errors or inconsistencies. A polished application reflects attention to detail, which is crucial for the role you're applying for.
How to prepare for a job interview at IQVIA
✨Know Your SAS Inside Out
As an Associate Principal Statistical Programmer, you'll need to demonstrate your expertise in SAS programming. Brush up on your knowledge of SAS Macros and be prepared to discuss specific projects where you've used these skills effectively.
✨Understand CDISC Standards
Familiarise yourself with CDISC standards such as CDASH, SDTM, and ADaM. Be ready to explain how you've applied these standards in previous roles, as this will show your understanding of regulatory requirements and their importance in clinical data submission.
✨Showcase Your Leadership Skills
Since the role involves leading programming activities, think of examples where you've successfully led a team or project. Highlight your ability to collaborate with cross-functional teams and how you ensured high-quality deliverables were met on time.
✨Prepare for Technical Questions
Expect technical questions related to statistical programming processes and quality control. Prepare to discuss your problem-solving approach and any challenges you've faced in past projects, along with how you overcame them.