The Senior Statistical Programmer will oversee the review of datasets, tables, figures, listings, and submission packages in submission-ready standard format (Adam). Additionally, they will deliver specialized guidance on the design, development, and quality control of SAS programs, which are used to access, extract, transform, review, analyze, and submit clinical data for all requested analyses.
Why Join IQVIA?
Partner with key figures in the healthcare sector to spearhead cutting-edge clinical initiatives.
Acquire experience across diverse therapeutic domains, indications, and clinical development stages.
We offer robust career development initiatives designed to support your professional growth in tandem with our company’s expansion. Through our AI-driven internal talent marketplace, employees gain access to personalized career advancement opportunities, enabling them to explore new roles, skills, and pathways aligned with their aspirations and organizational needs. Additionally, our dedicated Career Connections program provides structured support and resources to facilitate seamless transitions and long-term success within the organization.
Professional development opportunities are available company-wide through Employee Resource Groups, fostering mentorship and growth among employees.
We offer adaptable working arrangements to support both a healthy work–life balance and professional growth.
Join a company recognized as one of the 2026 Fortune World’s Most Admired Companies, a distinction earned for the fifth consecutive year.
Oversee and execute a broad spectrum of critical duties, including the systematic planning, organization, and supervision of project activities to ensure alignment with organizational objectives. Collaborate with cross-functional teams to facilitate seamless communication, resolve operational challenges, and drive efficiency across departments. Monitor progress through performance metrics, implement corrective measures when necessary, and report outcomes to senior leadership to support data-driven decision-making. Additionally, develop and maintain policies, procedures, and documentation to uphold compliance with industry regulations and internal standards.
Collaborates closely with study teams to develop data structures and specifications for various ad hoc and study deliverables, including Adam datasets, tables, figures, listings, and analysis submission content.
Works collaboratively with study teams to verify the integrity and correctness of clinical data—ensuring readiness for regulatory submission—as mandated by governing bodies (e.g., SDTM, Adam, tables, figures, listings, and define.xml specifications).
Leads and manages all requested pooled 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.
Drives the development and execution of in-house ISS and IS datasets and their related deliverables—including tables, figures, and listings—when external service providers (CRO’s) do not furnish these outputs.
Leads and directs the development and execution of sophisticated SAS programs specifically tailored for analyzing and reporting intricate clinical trial data structured in DISC Adam format.
Leads and manages the creation of global tools aimed at enhancing the efficiency and capacity of the Statistical Programming group.
Collaborates closely with clinical study teams to design and implement processes that maintain project timelines while ensuring high-quality deliverables.
Works in tandem with the CR&D team to address data analysis inquiries, ensuring alignment and accuracy in the delivery of requested insights.
Conducts supplementary statistical evaluations encompassing, but not limited to, a range of advanced analytical methods and techniques.
Respond to inquiries and requests from regulatory agencies promptly and thoroughly.
Prepare a comprehensive, integrated summary that evaluates both safety and efficacy metrics, ensuring all findings are clearly presented and thoroughly analyzed.
Provide assistance for the creation and dissemination of publications and presentations.
Facilitate the development of clinical trial plans and generate reports by conducting in-depth exploratory analyses of existing datasets.
Seeking a candidate with at least five years of experience in project management, preferably within the IT sector, and a proven ability to lead cross-functional teams to successful project completion. The ideal applicant will hold a Bachelor’s degree in a relevant field such as Computer Science, Engineering, or Business Administration. Strong proficiency in methodologies like Agile, Scrum, or Waterfall is essential, along with expertise in tools such as Jira, Trello, or Microsoft Project. Excellent communication skills, both written and verbal, are required to articulate project goals, progress, and challenges to stakeholders. The role demands a detail-oriented individual capable of managing multiple priorities under tight deadlines while maintaining a high standard of quality.
A Bachelor of Science degree in Computer Science, Mathematics, Statistics, or an equivalent discipline, along with practical experience in a relevant field, is required.
With a minimum of five years of hands-on experience in clinical programming or statistical programming within a CRO or pharmaceutical setting, proficiency in SAS Software is required.
A thorough knowledge of clinical programming and/or statistical programming methodologies and best practices is required.
Professionals with significant expertise in statistical programming via SAS software, encompassing both the creation and deployment of SAS Macros, are sought. The ideal candidate will demonstrate exceptional programming proficiency and analytical problem-solving abilities.
Proven expertise and practical experience in utilizing R Programming for statistical analysis and data manipulation are essential.
Proficiency in DISC standards, including CASH, SDTM, and Adam, is required.
With a demonstrated track record in spearheading programming initiatives for pooled and exploratory analyses within diverse clinical studies, as well as supporting submission-related activities (or comparable experience), you bring substantial expertise to this role.
Demonstrates strong capability to operate autonomously or collaboratively, achieving established objectives through self-directed time management.
Proficiency in collaborating within diverse, cross-functional, multicultural, and international clinical trial teams is required.
Qualifications
BA/BSc/HND
Experience Required
5 years
