Clinical SAS Programmer - ADaM & Regulatory Reports
AbbVie
AbbVie in North Chicago, IL is seeking a Statistical Programmer supporting clinical research. You'll develop and validate SAS programs for ADaM datasets, tables, listings, and figures, contributing to regulatory documentation. You'll consolidate diverse data sources, perform exploratory analyses and visualizations, and collaborate with Statistics, Data Strategy, Medical Writing, and Regulatory Publishing teams to ensure accurate, compliant analyses for drug development. #J-18808-Ljbffr AbbVie
- ...DescriptionMinimum 6 Years SAS Programming Experience supporting Phase 1-3 clinical trials in CRO or... ...understanding of SDTM and ADaM implementation guidance,... ...Figures for clinical study report using proc report or data _null_.Knowledge of regulatory submission process, experience...SASRegulatoryWork experience placement
- Role: Statistical Programmer supporting clinical research in AbbVie's pharmaceutical... ...focused on analysis and reporting of clinical trial data.... ...develop and validate SAS programs for creating ADaM datasets, Tables, Listings, Figures, and regulatory documentation...SASRegulatoryWork at office
- ...599 Responsibilities: The SAS/Statistical Programmer will also be responsible for... ...and consistency of clinical data. The successful candidate... ...clinical data analysis and reporting Develop and validate SAS programs... ...Ensure compliance with regulatory requirements and...SASRegulatory
- ...in the development of new pharmaceutical products. This exciting position involves leading statistical programming for clinical trials, developing SAS programs, and ensuring data integrity. Collaborate with a dynamic team of statisticians and data scientists while contributing...SAS
$78k - $156k
...Position Overview The Senior Non-Clinical Biostatistician applies... ...in the design, analysis, reporting, and internal publication of... ...matter expert in service of regulatory submissions, and liaise with... ...standard analysis software, e.g., SAS, R, Python. Apply excellent...SASRegulatoryWork at officeWorldwideNight shift$68k - $136k
...are used in hospitals, laboratories, and clinics around the globe. The crucial... ...The Software Engineer in Test (SET) reports into the AlinIQ Product Research and Development... ...allied documentation in conformance with regulatory, security, and privacy standards for all...RegulatoryWork experience placementWorldwide- .... Job Description The Manager, Clinical Data and Reporting Standards (CDARS) proactively participates... ...the assigned therapeutic areas: ADaM mapping and derivation Study-level... ...represented in a manner that support regulatory requirements to comply with CDISC...RegulatoryFull timeLocal area
- ...Senior Manager overseeing clinical data systems and team leadership... ...clinical trial data management and regulatory standards.... ...lead assigned team of direct reports Evaluate and implement clinical... ...experience ~ Intermediate SAS and/or SQL programming skills...SASRegulatory
- ...this role include the analysis and reporting of clinical trial data without supervision... ...activities for routine studies. Develop SAS programs for the creation of ADaM data sets following CDISC... ...integrated data. Create documentation for regulatory filings including reviewers...SASRegulatoryTemporary workLocal area3 days per week
- ...generate business value from clinical trials data. Our operational... ...responsibilities are achieved for direct reports. Provide training and... ...requirements, and applicable regulatory expectation Qualifications... ...Demonstrated intermediate SAS and/or SQL programming skills...SASRegulatory
- ...With deep domain expertise in regulatory sciences, clinical research solutions, quality... ..., including statistical reports, tables, listings, and graphs... .... Develop and maintain SAS programs for statistical... ...structures, such as SDTM and ADaM. We celebrate our differences...SASRegulatoryWork experience placementWork at officeRemote work
$115k - $155k
...to progress product concepts from early clinical need and technology exploration through... ...functional partners across R&D, Quality, Regulatory, Manufacturing, and Marketing to deliver... ...maintain technical documentation including reports, drawings, specifications, and analysis...RegulatoryWork at officeWorldwide$110k - $155k
...products meet performance requirements, regulatory requirements, and safety standardsDevelop... ...analysis of data and develop detailed reports documenting results, conclusions, and recommendationsCollaborate... ..., operations, project management, clinical) and ensure that products meet all...RegulatoryWork at officeWorldwideVisa sponsorship$78k - $156k
...hospitals, laboratories, and clinics around the globe. The crucial... ...validating software using R, SAS or other statistical software.... ...Participate in data review and regulatory submission.Propose recommendations... ...statistical concept and study report to cross-functional team and...SASRegulatoryWorldwideShift work- ...to provide statistical expertise across clinical trials and development. The role collaborates... ...to design analyses, ensure accurate reporting, and support publications while driving methodological... ...a PhD with 2+ years and proficiency in SAS, R, or Python to lead analyses and...SAS
$109.5k - $208.5k
...guides a team of Statistical Programmers in the research and development... ...Data Sciences, Medical Writing, Regulatory Publishing and Clinical Operations. Responsibilities... ...and oversees the development of SAS programs for the creation of ADaM data sets following CDISC...SASRegulatory$40 - $42 per hour
...support to the Global Epidemiology group in Clinical Sciences. This person will contribute to... ...diseases and indications contribute to regulatory submissions and responses and perform literature... ...using short-term studies/analyses SAS program experience required. Entry-...SASRegulatoryContract workTemporary workFor contractors$120k - $165k
...platforms.Collaborate with backend, web, UX, QA, cybersecurity, regulatory, and product stakeholders.Design and implement integrations... ...gateway integrations.Experience building secure communication, clinical communication, messaging, or alerting applications.Familiarity...RegulatoryFull timeTemporary workLocal areaWork visaFlexible hours$35 per hour
job summary: Are you a skilled Clinical Application Specialist seeking a high-impact, fully... ...key safety, risk management plans, and regulatory deliverables. qualifications:... ...related discipline. Strong proficiency in SAS programming; experience with SQL, R, or Python...SASRegulatoryHourly payContract workTemporary workWork experience placementRemote work- ...Programming to lead a team of statistical programmers in early development. You will guide SAS programming activities, ensure ADaM data sets following CDISC standards, and coordinate... ..., Data Sciences, Medical Writing and Regulatory Publishing. The role requires strong...SASRegulatory
- ...statisticians statistical programmers and AI specialists... ...on transforming clinical trial surveillance... ...and automated reporting. TSA delivers... ...migrating legacy SAS programs to R and... ...compliance with applicable regulatory requirements GCP... ...(e.g. CDISC SDTM/ADaM) and clinical...SASRegulatoryFull timeLocal area
- ...complexity of biological systems, the rigor of regulatory expectations, the pace of pipeline... ...-scale biologics portfolio spanning clinical, commercial, and lifecycle stages. Building... ..., regulatory submissions, technical reports, or equivalent — that demonstrates the ability...RegulatoryFull timeLocal area
$105k - $150k
...Write and coordinate technical documentation including protocols, reports, procedures, specifications, work instructions and original... ...and design excellence. Working with marketing, manufacturing, regulatory, and quality teams. Participating in cross-functional project...RegulatoryWork at officeWorldwideFlexible hours$42 - $46 per hour
...Description Job Description Job Title: Clinical Application Specialist I Job... ...Prefer candidate with clinical experience. SAS program experience required. Responsibilities... ...epidemiology data to core safety and regulatory documents, including RMPs and PSURs. Utilize...SASRegulatoryContract workTemporary workFor contractorsInternshipRemote work- ...AbbVie conducts ongoing clinical trial surveillance... ...statistical programming and reporting data integration data... ...integrated data on SDTM ADaM and integrated databases... ...trial monitoring or regulatory evidence generation.... ...). Familiarity with SAS. Experience leading...SASRegulatoryFull timeContract workLocal area
- ...equivalent)\n Integrate with front-office platforms, market/reference data, payments, SWIFT, CLS, GL/accounting, risk, and regulatory reporting \n Stay hands-on in the codebase while setting architectural standards for transaction integrity, idempotency, and...Regulatory
- ...that effort. \n \n This is an individual contributor role reporting to the SAP Team Manager, with no direct reports. It's best... ...engagements. \n Understanding of internal controls frameworks and regulatory compliance requirements. \n Experience with SAP Private...RegulatoryFull timeRelocation
$130k - $190k
...implementation planning, and change-risk management. \n Experience supporting Financial Markets, Market Risk, FRTB, Value at Risk, or Regulatory Reporting platforms. \n \n \n Compensation \n **Base salary range for this role is $130,000 - $190,000** \n Benefits \n \n...RegulatoryTemporary workRemote workWorldwide$96.8k - $145.2k
...cloud and platform innovation initiatives.Research, analyze, and report on disruptive technologies—such as Generative AI, Machine... ...Translate complex AI governance, cloud security guardrails, and regulatory requirements into practical technical specifications, partnering...RegulatoryFull timeSummer workWork at officeLocal areaFlexible hoursNight shift3 days per week- Planet Pharma is seeking a senior statistician to oversee all statistical planning and analyses for clinical programs. You will direct SAS programming across internal and external teams, lead statistical activities, and collaborate across trials (Phases I-III). A Master...SAS
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