The Senior Statistical Programmer will oversee the evaluation of datasets, ensuring they are prepared in submission-ready formats (Adam), alongside tables, figures, listings, and comprehensive submission packages. Additionally, the role involves delivering expert guidance in the design, development, and quality assurance of SAS programs, which are utilized to access, extract, transform, review, analyze, and submit clinical data for all required analyzes.
Why Join IQVIA?
Partner with esteemed professionals and key stakeholders to spearhead cutting-edge clinical initiatives at the vanguard of innovation.
Acquire experience across diverse therapeutic domains, indications, and clinical development stages.
Career development programs designed to expand alongside the organization, featuring AI-driven career progression via our internal talent marketplace, Career Connections.
Professional development and guidance can be accessed through various mentorship initiatives available company-wide, facilitated by Employee Resource Groups.
We offer flexible working arrangements designed to support both a healthy work–life balance and sustained professional achievement.
Join a company recognized among the 2026 Fortune World’s Most Admired Companies for the fifth consecutive year.
Oversee daily operations to ensure efficient workflow and adherence to established protocols, monitoring performance metrics to identify areas for optimization. Develop and implement strategic initiatives aimed at enhancing productivity, employee engagement, and overall operational excellence. Collaborate with cross-functional teams to align departmental goals with broader organizational objectives, fostering a culture of transparency and accountability. Provide leadership and mentorship to a team of professionals, delegating tasks effectively and empowering them to achieve their full potential while maintaining high standards of quality and professionalism.
Works collaboratively with study teams to develop data structures and specifications for both ad hoc deliverables and study outputs, such as Adam datasets, tables, figures, listings, and analysis submission content.
Collaborates closely with study teams to verify the integrity and precision of clinical data, ensuring readiness for regulatory submissions in adherence to established standards such as SDTM, Adam, and requirements for tables, figures, listings, and define.xml.
Leads and provides direction for pooled and exploratory analysis initiatives in close collaboration with the Statistics TA lead and/or study statisticians, as well as the clinical programming team and their repository of legacy data.
Experienced professionals in this role are responsible for directing and managing the development and execution of in-house ISS and IS datasets—notably tables, figures, and listings—when such deliverables are not supplied by an external Contract Research Organization (CRO).
Experienced professionals in this role will spearhead the development and execution of sophisticated SAS programs, specifically tailored to analyze and report intricate clinical trial data formatted in DISC Adam standards.
Leads and manages the creation of worldwide resources designed to enhance the efficiency and scalability of the Statistical Programming team.
Collaborates closely with clinical study teams to strategize and implement initiatives that ensure project timelines are achieved while maintaining high-quality outcomes.
Works collaboratively with the CR&D team to address and execute data analysis requests efficiently.
Conducts supplementary statistical analyses encompassing a broad range of procedures, such as but not limited to:
Provide assistance in addressing inquiries and requests received from regulatory agencies.
Prepare a comprehensive report that consolidates safety and efficacy data into a cohesive summary.
Assist in the development and dissemination of publications and presentations to effectively communicate key information and insights.
Facilitate the planning and reporting of clinical trials by conducting exploratory analyses of existing data sets.
Bachelor’s degree in computer science, engineering, or a related discipline is required. Candidates must have at least three years of experience in software development, with proficiency in programming languages such as Python, Java, or C++. Strong problem-solving skills and the ability to work collaboratively in a team environment are essential. Familiarity with version control systems, such as Git, and experience with Agile development methodologies are preferred. Excellent communication skills and a commitment to continuous learning are also required.
A bachelor’s degree in Computer Science, Mathematics, Statistics, or a closely related field, supplemented by pertinent professional experience, is required.
With a minimum of five years of professional expertise in clinical programming and/or statistical programming within a Contract Research Organization (CRO) or pharmaceutical setting, proficiency in SAS Software is required.
Individuals must possess a comprehensive grasp of clinical and/or statistical programming methodologies and the associated industry standards.
Professionals should possess advanced expertise in statistical programming within the SAS environment, encompassing the creation as well as application of SAS Macros. They must demonstrate robust programming capabilities and exceptional problem-solving aptitude.
Accumulated practical expertise in utilizing R Programming through comprehensive, hands-on training.
Proficiency in DISC standards, including CASH, SDTM, and Adam, is essential for this role.
Individuals should demonstrate a strong background in spearheading programming initiatives for pooled and exploratory analyses involving various clinical studies, as well as contributing to submission-related efforts.
Demonstrated capability to deliver results either autonomously or collaboratively, while maintaining accountability for personal deadlines and organizational objectives.
Proficiency in collaborating within diverse, cross-functional teams across international and multicultural clinical trial settings is required.
Qualifications
BA/BSc/HND
Experience Required
5 years
