IQVIA
Associate Director, Biostatistics - Global BIOS(m/w/x)
Vollzeit
mit Homeoffice
Senior
Keine Angabe
Frankfurt am Main
IQ
IQVIA6 Tage
Senior Statistical Programmer - FSP(m/w/x)
Vollzeit
mit Homeoffice
Senior
Keine Angabe
Frankfurt am Main
Nejo KI-Zusammenfassung
In this role, you will engage in a variety of tasks, including reviewing datasets and ensuring their submission readiness, leading complex analyses, and collaborating with study teams. Your expertise will help shape the quality and efficiency of clinical data reporting.
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Anforderungen
- •BSc in Computer Science, Mathematics, Statistics or related area
- •At least 5 years of experience in clinical programming or statistical programming
- •In-depth understanding of clinical programming and statistical programming processes
- •In-depth understanding of regulatory requirements relevant to statistical programming
- •Extensive experience with statistical programming using SAS software
- •Strong programming and problem-solving skills
- •Advanced knowledge in CDISC standards (CDASH, SDTM, ADaM)
- •Proven experience in leading programming activities for clinical studies
- •Ability to work effectively independently or in a team setting
- •Experience in cross-functional, multicultural and international clinical trial teams
Bachelor-Abschluss
Berufserfahrung
5 Jahre
Deine Aufgaben
- •Review datasets in submission-ready standard format (ADaM)
- •Create tables, figures, listings, and submission packages
- •Collaborate with study teams to design data structures and specifications
- •Ensure quality and accuracy of clinical data for submission readiness
- •Lead pooled and exploratory analyses with Statistics TA lead and study statisticians
- •Oversee in-house specification and delivery of ISS and ISE datasets
- •Design and implement complex SAS programs for clinical trial data analysis
- •Develop global tools to enhance efficiency in the Statistical Programming group
- •Plan and execute activities with clinical study teams to meet project timelines
- •Collaborate with CR&D staff on data analysis requests
- •Perform additional statistical analyses to support regulatory agency responses
- •Generate integrated summaries of safety and efficacy
- •Support publications and presentations
- •Conduct exploratory analyses for planning and reporting of clinical trials
Tools & Technologien
SAS
Sprachen
Englisch – verhandlungssicher
Deine Vorteile
Flexibles Arbeiten
- •Home-based remote work opportunities
Familienfreundlichkeit
- •Great work/life balance
Lockere Unternehmenskultur
- •Collaborative team environment
Sicherer Arbeitsplatz
- •Job stability
Karriere- und Weiterentwicklung
- •Career advancement opportunities
Die Originalanzeige dieses Stellenangebotes in der aktuellsten Version findest du hier. Nejo hat diesen Job automatisch von der Website des Unternehmens IQVIA erfasst und die Informationen auf Nejo mit Hilfe von KI für dich aufbereitet. Trotz sorgfältiger Analyse können einzelne Informationen unvollständig oder ungenau sein. Bitte prüfe immer alle Angaben in der Originalanzeige! Inhalte und Urheberrechte der Originalanzeige liegen beim ausschreibenden Unternehmen.
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