The Senior Statistical Programmer will oversee datasets in submission-ready Adam format, along with tables, figures, listings, and submission packages. They will deliver specialized guidance in the design, execution, and quality assurance of SAS programs, enabling the access, extraction, transformation, review, analysis, and submission of clinical data for all necessary analyses.
Why Join IQVIA?
Partner with leading professionals in the industry to drive forward-thinking clinical projects that set new benchmarks in innovation.
Acquire experience across diverse therapeutic domains, indications, and clinical trial phases to broaden your expertise in medical research and development.
We offer robust career development prospects to support both personal and organizational growth, leveraging AI-driven career progression via our internal talent marketplace, Career Connections.
Mentorship prospects are offered throughout the organization through Employee Resource Groups, fostering professional growth and collaboration among employees.
Flexible working arrangements are offered to foster a balanced work–life integration, thereby enhancing both personal well-being and professional achievement.
Join a company ranked among the 2026 *Fortune* World’s Most Admired Companies for the fifth consecutive year.
Responsibilities
Works closely with study teams to establish the data framework and detailed specifications for various ad hoc and study deliverables, such as Adam datasets, tables, figures, listings, and analysis submission content.
Collaborates closely with study teams to guarantee the integrity and precision of clinical data, ensuring its readiness for submission to regulatory authorities in accordance with specified standards such as SDTM, Adam, tables, figures, listings, and define.xml.
Experienced professionals will spearhead and manage pooled and exploratory analysis initiatives in close collaboration with the Statistics TA lead, study statisticians, and the clinical programming team, leveraging their extensive legacy data resources to deliver comprehensive insights.
Experienced professionals in this role will direct and manage 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).
Experienced professionals in this role will spearhead the creation and execution of sophisticated SAS programs specifically engineered to process and analyze intricate clinical trial data formatted in DISC Adam standards. This position involves guiding project teams through the full development lifecycle, from initial design phases to final implementation, ensuring seamless integration and compliance with regulatory and industry requirements.
Oversees and directs the creation of worldwide solutions aimed at enhancing the efficiency and productivity of the Statistical Programming team.
Collaborates closely with clinical study teams to develop and implement strategies that ensure project timelines are consistently met while maintaining the highest standards of deliverable quality.
Works in conjunction with the CR&D team to address data analysis inquiries submitted to the department.
Conducts supplementary statistical evaluations encompassing, without limitation, a diverse array of analytical methodologies to derive meaningful insights from data sets.
Provide assistance in addressing inquiries and submissions from regulatory agencies, ensuring timely and accurate responses in adherence to applicable guidelines and requirements.
Integrate comprehensive assessments of safety and efficacy to produce a cohesive and detailed summary, ensuring all critical data points are accurately captured and analyzed. This role requires meticulous attention to detail, strong analytical skills, and the ability to synthesize complex information into clear, actionable insights. Proficiency in data evaluation, regulatory knowledge, and scientific writing is essential, along with experience in clinical or medical research environments. Collaborate with cross-functional teams to validate findings, address discrepancies, and maintain alignment with established protocols and guidelines.
Provide assistance in the preparation and dissemination of reports, articles, and other written materials, as well as the development and delivery of visual and oral presentations to various audiences.
Conduct exploratory analyses of existing clinical trial data to assist in the planning and reporting phases of study execution.
Seeking a highly motivated individual with exceptional organizational skills and a strong attention to detail to oversee administrative operations. The ideal candidate will possess a minimum of three years of relevant experience, proficiency in Microsoft Office Suite, and the ability to manage multiple priorities in a fast-paced environment. Responsibilities include coordinating schedules, preparing reports, and ensuring seamless communication between departments. Candidates must demonstrate excellent written and verbal communication skills, as well as a commitment to maintaining confidentiality and adhering to company policies.
A bachelor’s degree in Computer Science, Mathematics, Statistics, or a closely related field, supplemented by applicable professional experience, is required.
With a minimum of five years of hands-on experience in either clinical or statistical programming within the contract research organization (CRO) or pharmaceutical sector, and proficiency in SAS Software, you will be a strong candidate for this role.
A comprehensive grasp of clinical programming methodologies and statistical programming guidelines is essential.
Professionals must possess advanced expertise in statistical programming with SAS, encompassing both macro development and utilization. Demonstrated proficiency in programming and adept problem-solving abilities are essential.
Possesses comprehensive, practical experience with R Programming through extensive training or hands-on application.
Proficiency in DISC standards, including CASH, SDTM, and Adam, is essential.
With a strong track record, you will have led programming initiatives for combined and exploratory analyses across various clinical studies and submission processes (or similar experience).
Demonstrates a strong capacity to thrive in both independent and collaborative environments while consistently achieving established objectives through self-directed time management.
Seasoned professionals with a track record of collaborating effectively within diverse, cross-functional, multicultural, and international clinical trial teams are encouraged to apply.
Qualifications
BA/BSc/HND
Experience Required
5 years
