Philippines - Makati Cityfull timeSenior
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query:Statistical Science Lead
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US - Gaithersburg - MDfull timeDirector
verified Aug 4, 2026posted 4 months ago
US - Gaithersburg - MDfull timeDirector$188.3K–282.4K
posted 22 days ago
Job Openings Senior Statistical Programmer About the job Senior Statistical Programmer Job Title: Senior Statistical Programmer Job Location: Durham, North Carolina, United States of America Job Location Type: Remote Job Contract Type: Full-time Job Seniority Level: Essential Functions of the Job (Key responsibilities)Conduct statistical programming work of clinical data using SAS Software.Ensure that all programs, outputs and documentation are consistent with ICH guidelines and are conducted in compliance with company SOPs.Generate analysis datasets according to CDISC standard and SAP.Implement analysis methods according to SAP, and produce summary tables, graphs and data listings using SAS; Conduct adhoc analyses.Validate programs and associated results produced by other programming colleagues.Participate in TLF shell preparation and review, and assist statistician for SAP preparation.Run CDISC validation programs e.g. OpenCDISC reports to ensure ADaM datasets are CDISC compliant.Learn, and implement Incyte standard SAS macros for efficient analyses of clinical data supervised by Lead programmers.Work independently to program for individual studies with minimum supervision.Check that the validation summary reports are clean of errors and warnings, and show proper documentation of SAS programs.Review individual study CDISC validation output.Qualifications (Minimal acceptable level of education, work experience, and competency)BA/BS degree in mathematics, statistics, computer science or health related field. Or equivalent experience4 – 8 years of SAS programming working experience in the pharmaceutical industry.Good SAS programming skills and attention to detailsDemonstrated knowledge of regulatory guidelines, including electronic submission standards.Strong organizational, time management, communication, and project coordination and leadership skills.Must be able to work well under timeline pressure.Must be able to work on multiple tasks while coordinating others at the same time.IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.comIQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoeIQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.The potential base pay range for this role, when annualized, is $88,300.00 - $220,900.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.This job is curated by Lifelancer. Lifelancer is a talent-hiring platform in Life Sciences, Pharma and IT. The platform connects talent with opportunities in pharma, biotech, health sciences, healthtech and IT domains. Please apply via Lifelancer platform to get connected to the application page and to find similar roles. Apply for Position Or refer someone Share Facebook Line LinkedIn X (Formerly Twitter) Whatsapp EmailRemoteSenior
posted 10 days ago
India - Bangalorefull timeSenior
verified Jun 8, 2026posted 4 months ago
Spain - Barcelonafull timeSenior
verified Jun 12, 2026posted 3 months ago
Toranomon (NPKK Head Office)full timeSenior
verified Jun 13, 2026posted 4 months ago
United StatesSenior
verified Jun 18, 2026posted 4 months ago
Remote, United StatesRemoteSenior$185K–230K
posted 2 months ago
Chiyoda, Tokyo, Japanfull timeSenior
verified Jun 13, 2026posted 3 months ago
Bangalore, India
posted 2 months ago
London, United Kingdomfull timeSenior£49.1K–91.3K
posted 2 months ago
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posted 18 days ago
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United StatesSenior
verified Jun 18, 2026posted 3 months ago
Bangalore, IndiaSenior
verified Jun 20, 2026posted 4 months ago
$189.4K
posted 10 days ago
Job Openings Principal Statistical Programmer About the job Principal Statistical Programmer Job Title: Principal Statistical Programmer Job Location: Durham, North Carolina, United States of America Job Location Type: Remote Job Contract Type: Full-time Job Seniority Level: Position SummaryWe are seeking a Principal Statistical Programmer to provide full end‑to‑end statistical programming support across clinical development programs. This role requires deep technical expertise, leadership, and hands‑on delivery, covering SDTM, ADaM, TLF development, and regulatory submission support. The Principal Statistical Programmer will serve as a subject matter expert, ensure high‑quality deliverables, and contribute to programming standards and best practices.Key ResponsibilitiesProvide end‑to‑end statistical programming support for clinical studies from study setup through submissionLead and perform development and validation of:SDTM datasetsADaM datasetsTables, Listings, and Figures (TLFs)Ensure all deliverables are compliant with CDISC standards and regulatory requirementsSupport regulatory submissions (e.g., FDA, EMA), including define.xml, submission‑ready datasets, and reviewer’s guidesServe as a Principal‑level programmer, providing technical leadership and guidance to other programmers as neededContribute to and help maintain programming standards, macros, and validation processesReview and approve programming deliverables to ensure accuracy, consistency, and qualityCollaborate closely with Biostatistics, Data Management, Clinical Operations, and Regulatory teamsProactively identify risks and propose efficient, compliant solutions within timelinesRequired QualificationsBachelor’s or Master’s degree in Statistics, Mathematics, Computer Science, Life Sciences, or related fieldExtensive experience as a statistical programmer, with demonstrated Principal‑level responsibilitiesStrong hands‑on experience with:SDTM and ADaM dataset developmentTLF programmingRegulatory submission deliverablesExpert proficiency in base SAS and Advanced SAS with good hands on SAS MacrosIn‑depth knowledge of CDISC standards, regulatory guidelines, and submission requirementsProven ability to manage complex studies independently from start to finishIQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.comIQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoeIQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.The potential base pay range for this role, when annualized, is $98,200.00 - $273,200.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.This job is curated by Lifelancer. Lifelancer is a talent-hiring platform in Life Sciences, Pharma and IT. The platform connects talent with opportunities in pharma, biotech, health sciences, healthtech and IT domains. Please apply via Lifelancer platform to get connected to the application page and to find similar roles. Apply for Position Or refer someone Share Facebook Line LinkedIn X (Formerly Twitter) Whatsapp EmailRemotePrincipal
posted 10 days ago
United StatesSenior
verified Jun 20, 2026posted 3 months ago
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