The Senior Statistical Programmer will oversee the verification and preparation of datasets in submission-ready formats (Adam), as well as tables, figures, listings, and submission packages. Additionally, they will bring specialized knowledge to the design, development, and quality assurance of SAS programs, which are used to access, extract, transform, review, analyze, and submit clinical data for all specified analyzes.
Why Join IQVIA?
Partner with pioneering figures in the sector to spearhead transformative clinical projects, driving innovation at the cutting edge of the field.
Acquire insight into diverse therapeutic domains, indications, and clinical development stages.
We offer robust career development initiatives designed to support your growth alongside the company’s expansion, featuring AI-driven career advancement through our proprietary internal talent marketplace, Career Connections.
Mentorship initiatives are available throughout the organization through Employee Resource Groups, fostering professional growth and development.
We offer flexible working arrangements to support a healthy work–life balance and foster professional growth.
Join an organization recognized as one of the 2026 Fortune World’s Most Admired Companies—nominated for an unprecedented fifth consecutive year.
Responsibilities
Works closely with study teams to develop data structures and detailed specifications for ad hoc deliverables as well as study outputs, such as Adam datasets, tables, figures, listings, and analysis submission content.
Collaborates closely with study teams to verify clinical data meets rigorous quality and accuracy standards, ensuring submissions align with regulatory requirements—including SDTM, Adam, tables, figures, listings, and define.xml.
Leads and manages pooled and exploratory analysis initiatives, collaborating closely with the Statistics TA lead and/or study statisticians, as well as the clinical programming team and their repository of legacy data.
Leads and manages 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 oversees the design and implementation of complex SAS programs for applications designed to analyze and report complex clinical trial data in CDISC ADaM format
Drives the design and implementation of worldwide tools to enhance the efficiency and capacity of the Statistical Programming team.
Collaborates closely with clinical study teams to plan and implement activities that ensure project timelines are met while maintaining high-quality deliverables.
Collaborates closely with CR&D staff to address and fulfill data analysis requests.
Conducts supplementary statistical evaluations encompassing, but not limited to, a broad range of analytical methods and approaches.
Provide assistance in addressing inquiries from regulatory bodies, ensuring timely and accurate communication while maintaining compliance with applicable standards and guidelines.
Craft a comprehensive, integrated overview encompassing safety and efficacy data.
Provide assistance with the preparation and dissemination of publications and presentations.
Assist in the development and oversight of clinical trial plans by conducting exploratory data analyses to generate insights from existing datasets.
We’re seeking a skilled professional to join our team, requiring a minimum of five years of relevant experience in the field. Candidates must possess strong analytical abilities, exceptional communication skills, and proficiency in industry-standard software. Additionally, a bachelor’s degree in a related discipline or equivalent work experience is essential. The ideal applicant will demonstrate a proven track record of delivering results under tight deadlines while maintaining meticulous attention to detail. Familiarity with current trends and best practices in the sector is also required to ensure success in this role.
A Bachelor of Science degree in Computer Science, Mathematics, Statistics, or a closely related field, supported by pertinent professional experience, is required.
Professionals with a minimum of five years of hands-on experience in either clinical programming or statistical programming, specifically within a Contract Research Organization (CRO) or pharmaceutical setting, and proficiency in SAS Software, are encouraged to apply.
Proficient knowledge of clinical and/or statistical programming methodologies, frameworks, and best practices is required.
Professionals should possess significant expertise in statistical programming with SAS, encompassing both the creation and implementation of SAS Macros. Additionally, candidates must demonstrate exceptional programming proficiency alongside robust problem-solving capabilities.
Possesses comprehensive, practical training and hands-on experience utilizing R Programming.
Proficiency in DISC standards, including CASH, SDTM, and Adam, is essential for this role.
With a strong track record, candidates should demonstrate expertise in directing programming efforts for pooled and exploratory analyses across various clinical studies, as well as submission initiatives—or comparable experience.
Demonstrated proficiency in collaborating seamlessly within team environments while also excelling in independent work, coupled with the capacity to achieve established objectives through disciplined self-management of schedules.
Proficiency in collaborating within diverse, cross-functional, multicultural, and globally dispersed clinical trial teams is essential.
Qualifications
BA/BSc/HND
Experience Required
5 years
