The Senior Statistical Programmer will oversee the validation of datasets formatted to submission standards (Adam), along with tables, figures, listings, and submission packages. Additionally, this role involves delivering specialized guidance in the design, execution, and quality assurance of SAS programs, which are employed to access, extract, transform, review, analyze, and submit clinical data for all required analyzes.
At IQVIA, we invite professionals to become part of a dynamic and forward-thinking organization that drives innovation in healthcare and life sciences. Our team collaborates across diverse functions to deliver cutting-edge solutions that enhance patient outcomes and streamline industry operations. By joining us, you’ll engage with transformative technologies, work alongside industry leaders, and contribute to meaningful projects that shape the future of global healthcare. We foster a culture of continuous learning, creativity, and accountability, ensuring every employee has the opportunity to grow both personally and professionally.
Partner with pioneering clinical innovators to spearhead groundbreaking projects within the industry.
Acquire insights into diverse therapeutic domains, indications, and clinical development stages to broaden your expertise and understanding of the pharmaceutical landscape.
We provide numerous career development opportunities to foster both personal and organizational growth, including AI-driven career advancement via our internal talent marketplace, Career Connections.
Explore diverse mentorship prospects throughout the organization through the Employee Resource Groups, fostering professional growth and collaboration.
Accommodating work arrangements are offered to support the harmonization of professional achievements with personal life commitments.
Join an elite organization recognized among the 2026 Fortune World’s Most Admired Companies, a distinction achieved through five consecutive years of nomination.
Responsibilities
Works collaboratively with study teams to develop data structures and detailed specifications for various ad hoc and study deliverables, such as Adam datasets, tables, figures, listings, and analysis submission content.
Works collaboratively with study teams to verify that clinical data meets stringent quality and accuracy standards, ensuring submissions are prepared in full compliance with regulatory requirements such as SDTM, Adam, tables, figures, listings, and define.xml.
Experienced professionals in this role will provide direction and management for pooled and exploratory analysis initiatives, collaborating closely with the Statistics TA lead and/or designated study statisticians, as well as interfacing effectively with the clinical programming team to process and integrate legacy data.
Experienced professionals are responsible for 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 outputs are not furnished by the Contract Research Organization (CRO).
Leads and manages the development and execution of intricate SAS programs, ensuring they effectively analyze and report complex clinical trial data formatted in DISC Adam.
Leads and directs the creation of comprehensive global tools, enhancing the efficiency and capacity of the Statistical Programming group.
Collaborates closely with clinical study teams to develop and implement strategic plans, ensuring project milestones are achieved while maintaining the highest standards of quality in all deliverables.
Works in partnership with the CR&D team to address and fulfill data analysis requests.
Conducts supplementary statistical evaluations encompassing a broad range of methodologies, including but not limited to:
Provide assistance in generating responses to inquiries from regulatory agencies.
Develop a comprehensive, cohesive summary detailing safety and efficacy outcomes, ensuring thorough integration of all relevant data and findings.
Provide assistance in the development and dissemination of publications and presentations.
Assist in the strategic planning and reporting of clinical trials by conducting exploratory analyses of the existing data.
Candidates must fulfill the following criteria: a bachelor’s degree in computer science, engineering, or a related technical field; at least five years of experience in software development; proficiency in programming languages such as Java, Python, or C++; and strong problem-solving and analytical skills. Familiarity with cloud platforms like AWS or Azure, as well as experience with DevOps practices and CI/CD pipelines, is highly desirable. Excellent communication abilities and the capacity to collaborate effectively within cross-functional teams are essential.
A Bachelor’s degree in Computer Science, Mathematics, Statistics, or a closely related field, coupled with applicable professional experience, is required.
With a minimum of five years of direct experience in clinical programming, statistical programming, or both, within the CRO or pharmaceutical sector and utilizing SAS Software, you will be well-prepared for this role.
Proficiency in clinical and/or statistical programming methodologies and established industry standards is essential.
Professionals should possess significant expertise in statistical programming with the SAS software, encompassing both the development and utilization of SAS Macros. They must demonstrate advanced programming abilities and a keen aptitude for problem-solving.
Experienced in utilizing R Programming through practical, hands-on application.
Proficiency in DISC standards, including CASH, SDTM, and Adam, is required.
Demonstrated expertise in directing programming initiatives for pooled and exploratory analyses across various clinical studies, as well as submission-related activities, is required.
Demonstrated capability to deliver results efficiently in both autonomous and collaborative environments while adhering to established deadlines through self-directed time management.
Experienced in collaborating within diverse, cross-functional clinical trial teams, including multicultural and international members.
Qualifications
BA/BSc/HND
Experience Required
5 years
