Find a job 
Featured Companies 
Featured Universities 
For Companies At a Glance
- Tasks: Lead statistical programming for clinical trials, ensuring data quality and submission readiness.
- Company: IQVIA is a global leader in clinical research services, enhancing healthcare through innovative solutions.
- Benefits: Enjoy remote work, great work/life balance, career advancement, and collaboration with industry leaders.
- Why this job: Join a dynamic team reshaping healthcare while working on impactful projects in a supportive environment.
- Qualifications: BSc in relevant field with 5+ years of experience in statistical programming using SAS.
- Other info: Work with top pharmaceutical clients and gain exposure to various therapeutic areas.
The predicted salary is between 42000 - 84000 £ per year.
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 plans and executes 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:
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
#J-18808-Ljbffr
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 importance of ADaM datasets and CDISC standards, as these are crucial for the position. This knowledge will help you speak confidently about your expertise during interviews.
✨Tip Number 2
Network with professionals in the clinical programming field, especially those who work at IQVIA or similar companies. Attend industry conferences or webinars to connect with potential colleagues and learn more about the company culture and expectations.
✨Tip Number 3
Prepare to discuss your experience with SAS programming in detail. Be ready to provide examples of complex projects you've worked on, particularly those involving pooled and exploratory analyses, as this will demonstrate your capability to handle the responsibilities of the role.
✨Tip Number 4
Research IQVIA's recent projects and initiatives in the pharmaceutical sector. Being knowledgeable about their work will not only impress your interviewers but also allow you to tailor your responses to show how you can contribute to their ongoing success.
We think you need these skills to ace Senior Statistical Programmer (Remote - Permanent Homebased)
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant experience in statistical programming and clinical data analysis. Emphasise your proficiency with SAS software and any experience you have with CDISC standards, as these are crucial for the role.
Craft a Compelling Cover Letter: In your cover letter, express your passion for the pharmaceutical industry and your desire to contribute to advancing therapies. Mention specific projects or experiences that demonstrate your ability to lead programming activities and collaborate effectively with study teams.
Showcase Your Problem-Solving Skills: Provide examples in your application of how you've tackled complex programming challenges in the past. Highlight your analytical skills and your ability to deliver high-quality results under tight deadlines.
Highlight Team Collaboration: Since the role involves working closely with cross-functional teams, make sure to mention your experience in collaborative environments. Discuss how you've successfully worked with diverse teams to meet project goals and timelines.
How to prepare for a job interview at IQVIA
✨Know Your SAS Inside Out
As a Senior Statistical Programmer, you'll need to demonstrate your expertise in SAS programming. Brush up on your skills, especially with 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 knowledge is crucial for ensuring submission readiness of clinical data.
✨Showcase Your Collaborative Spirit
This role involves working closely with study teams and other stakeholders. Prepare examples that highlight your ability to collaborate effectively in cross-functional teams, especially in a multicultural and international context.
✨Prepare for Regulatory Discussions
Since the position requires an understanding of regulatory requirements, be prepared to discuss your experience with GCP and ICH guidelines. Think of instances where you’ve had to address regulatory queries or ensure compliance in your programming work.
