The Senior Statistical Programmer will oversee the validation and preparation of datasets, tables, figures, listings, and submission packages in submission-ready formats (Adam). Additionally, the incumbent will offer specialized guidance in designing, developing, and ensuring the quality control of SAS programs, which are utilized to access, extract, transform, review, analyze, and submit clinical data for all required analyzes.
Why choose to join VIA?
Partner with leading figures in the industry to spearhead initiatives at the cutting edge of clinical advancement.
Acquire insights into diverse therapeutic domains, indications, and clinical development stages.
Professional growth is encouraged as the organization expands, supported by AI-driven career progression via an internal talent platform, Career Connections.
Mentorship opportunities are available throughout the organization through Employee Resource Groups.
We prioritize adaptable work arrangements to support both a healthy work–life balance and sustained 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.
Responsibilities
Works collaboratively with study teams to establish the framework for data structures and detailed specifications required for ad hoc analyses, study deliverables, and regulatory submissions, encompassing Adam datasets, tables, figures, listings, and other analysis-related content.
Collaborates closely with study teams to uphold the integrity and precision of clinical data, ensuring its readiness for regulatory submission in accordance with established standards (e.g., SDTM, Adam, tables, figures, listings, define.xml).
Leads and manages all requested activities for 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.
Leads and manages the internal development and execution of ISS and IS datasets, along with their associated 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 conception and execution of sophisticated SAS programs, specifically designed to analyze and generate reports from intricate clinical trial data presented in DISC Adam format.
Oversees and directs the creation of comprehensive global tools, designed to enhance the efficiency and capacity of the Statistical Programming team.
Collaborates closely with clinical study teams to strategize and implement initiatives, ensuring project milestones are achieved while maintaining stringent quality standards.
Works collaboratively with the CR&D team to address and fulfill data analysis requests.
Conducts supplementary statistical evaluations encompassing, but not limited to, the following tasks:
Respond promptly and accurately to inquiries from regulatory agencies, ensuring all communications adhere to established guidelines and timelines. Collaborate with cross-functional teams to gather necessary documentation and data, facilitating comprehensive and compliant responses. Maintain meticulous records of all interactions and submissions to ensure transparency and accountability. Stay informed about evolving regulatory requirements to proactively address potential inquiries and mitigate risks.
Prepare a cohesive evaluation of safety and efficacy data, synthesizing findings into a clear and comprehensive summary to support informed decision-making and regulatory compliance.
Provide assistance in the development and dissemination of publications and presentations to ensure effective communication of key information and findings.
Assist in the planning and reporting of clinical trials by conducting exploratory analyses of existing data to derive meaningful insights.
Seeking a highly motivated professional with a minimum of five years of relevant experience in a related field. Candidates must possess strong analytical and problem-solving skills, along with the ability to work both independently and collaboratively in a fast-paced environment. Proficiency in industry-standard software and tools is essential, and familiarity with current trends and best practices is required. Excellent communication and organizational abilities are also necessary to effectively manage multiple tasks and meet deadlines. A bachelor’s degree in a relevant discipline or an equivalent combination of education and experience is preferred.
A bachelor’s degree in Computer Science, Mathematics, Statistics, or a closely related field, accompanied by pertinent professional experience, is required.
We seek candidates with a minimum of five years of hands-on experience in clinical programming and/or statistical programming within the CRO or pharmaceutical sector, utilizing SAS software proficiently.
A comprehensive grasp of clinical programming principles and/or statistical programming methodologies and established standards is essential.
Professionals with advanced proficiency in statistical programming, specifically leveraging SAS software, are sought, with an emphasis on both the development and implementation of SAS Macros. The ideal candidate will demonstrate exceptional programming capabilities alongside robust problem-solving expertise to address complex analytical challenges.
Proficient in R Programming with practical, hands-on training and experience.
Proficiency in DISC standards, including CASH, SDTM, and Adam, is essential for this role.
With a strong track record, you will have led programming initiatives for pooled and exploratory analyses spanning multiple clinical studies, as well as submission-related tasks—or demonstrated equivalent expertise.
Demonstrated capacity to thrive in both autonomous and collaborative environments, delivering results by prioritizing individual responsibilities and adhering to established deadlines.
Professional experience collaborating within diverse, cross-functional teams on multicultural and international clinical trial initiatives is required.
Qualifications
BA/BSc/HND
Experience Required
5 years
