The Senior Statistical Programmer will oversee the validation of datasets formatted to submission-ready standards (Adam), as well as tables, figures, listings, and submission packages. Additionally, this role will involve offering specialized guidance in the design, execution, and quality assurance of SAS programs, which are utilized to access, extract, transform, review, analyze, and submit clinical data for all specified analyzes.
Why Join IQVIA?
Partner with leading figures in the industry to spearhead groundbreaking clinical initiatives.
Acquire insight into diverse therapeutic domains, indications, and clinical development stages to broaden your understanding of the pharmaceutical landscape. This opportunity will immerse you in multiple therapeutic areas while exposing you to varied indications and the intricacies of different clinical trial phases.
As you progress in your role, you’ll benefit from abundant career development prospects designed to expand alongside the organization’s growth. Our advanced internal talent marketplace employs AI to facilitate personalized career advancement, ensuring your professional journey aligns with evolving goals. Additionally, the Career Connections program offers structured pathways to enhance skills and foster meaningful connections within the company.
Employees can engage in mentorship programs facilitated by Employee Resource Groups throughout the organization.
We offer adaptable working arrangements to support a harmonious work–life balance and foster professional excellence.
Join an organization recognized among the 2026 Fortune World’s Most Admired Companies, distinguished for securing this prestigious nomination for the fifth consecutive year.
Our role encompasses a range of core duties, including the coordination and execution of multifaceted projects to ensure timely completion within budgetary constraints. You will be responsible for overseeing daily operations, fostering collaboration across departments, and implementing strategies that enhance productivity and efficiency. Additionally, the position involves analyzing performance metrics, identifying areas for improvement, and presenting actionable recommendations to senior leadership. Strong leadership and problem-solving skills will be essential in guiding teams through challenges while maintaining high standards of quality and accountability.
Partners with study teams to establish data structures and detailed specifications for both ad hoc requests and study deliverables, encompassing Adam datasets, Tables, Figures, Listings, and Analysis Submission content.
Works collaboratively with study teams to maintain the integrity and precision of clinical data, ensuring it meets regulatory submission standards such as SDTM, Adam, and deliverables including tables, figures, listings, and define.xml.
Leads and directs all requested initiatives for comprehensive and exploratory analyses, collaborating closely with the Statistics TA lead and/or study statisticians, as well as the clinical programming team and their repository of legacy data.
The position involves directing and managing the internal development and execution of ISS and IS datasets, along with their related deliverables—such as tables, figures, and listings—when these are not furnished by the Contract Research Organization (CRO).
Leads and manages the entire process of designing and executing sophisticated SAS programs specifically tailored for analyzing and reporting intricate clinical trial data formatted in DISC Adam standards.
Oversees the strategic development and implementation of global tools aimed at enhancing efficiency and capacity within the Statistical Programming group.
Collaborates closely with clinical study teams to strategize, implement, and oversee activities, ensuring project milestones are achieved while maintaining stringent quality standards in all deliverables.
Works collaboratively with the CR&D team to address data analysis inquiries.
Conducts supplementary statistical evaluations encompassing, but not limited to, the following tasks:
Provides assistance with preparing and submitting responses to regulatory agencies as needed.
Produce a comprehensive evaluation summarizing safety and efficacy data through integrated analysis.
Assist in the development and dissemination of publications and presentations to ensure accurate and timely delivery of information. Collaborate with team members to review, edit, and format content in alignment with organizational standards. Contribute to the creation of compelling visuals and supporting materials to enhance audience engagement and understanding. Maintain consistency in branding and messaging across all communication materials. Track deadlines and milestones to ensure projects are completed efficiently and meet quality expectations.
Facilitate the planning and reporting of clinical trials by conducting exploratory analyses of existing data.
Seeking a highly motivated individual with a minimum of 5 years of experience in a similar role, preferably in a fast-paced environment. The ideal candidate must possess strong analytical skills, excellent communication abilities, and proficiency in relevant software or tools. A bachelor’s degree in a related field is required, and relevant certifications are a plus. Additionally, the candidate should demonstrate a proven track record of meeting deadlines, managing multiple priorities, and working effectively both independently and as part of a team.
A bachelor’s degree in Computer Science, Mathematics, Statistics, or a closely related discipline, supplemented by applicable professional experience, is required.
With a minimum of five years of experience in clinical or statistical programming within the CRO or pharmaceutical sector, utilizing SAS software, the ideal candidate will have a strong background in this field.
Individuals should possess a comprehensive grasp of clinical and statistical programming methodologies and associated industry standards.
Professionals should possess comprehensive expertise in statistical programming with SAS software, encompassing both the creation and utilization of SAS Macros. They must demonstrate exceptional programming proficiency alongside advanced problem-solving capabilities.
Experienced in R Programming through practical application and hands-on training.
Demonstrates comprehensive expertise in DISC standards, specifically CASH, SDTM, and Adam, ensuring alignment with industry best practices and regulatory requirements.
Delivers demonstrated expertise in directing programming initiatives for pooled and exploratory analyses spanning numerous clinical studies, as well as submission-related processes, or equivalent background.
Demonstrated capacity to work autonomously or collaboratively while delivering results within established deadlines.
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Proficiency in collaborating within diverse, cross-functional teams across multicultural and international settings within clinical trials is essential.
Qualifications
BA/BSc/HND
Experience Required
5 years
