Du entwickelst und pflegst statistische Modelle und Programme, überprüfst Dokumente und unterstützt Projekte zur Datenvisualisierung.
Anforderungen
- •Bachelor’s or Master’s Degree in Computer Science
- •At least 5 years experience in SAS programming
- •Advanced proficiency in SAS programming
- •Basic understanding of statistical methods
- •Thorough knowledge of CDISC standards
- •Knowledge of ICH-GCP regulations
- •Experience in outsourced working environments
Deine Aufgaben
- •Entwickeln und Pflegen von SDTMs, ADaMs, TFLs
- •Überprüfen von Programmdokumenten wie SAP und TFLs
- •Entwickeln und Validieren von SAS-Programmen und -Makros
- •Planen und Durchführen von Validierungs-QC-Aktivitäten
- •Unterstützen bei der Entwicklung von Datenrepositories
- •Entwickeln von Datenvisualisierungs- und Explorationswerkzeugen
Original Beschreibung
# Senior Statistical Analyst (m/f/d)
Country:
Germany
City:
Aachen
Department:
Research & Development
Job ID:
44576
Professional | Permanent | Full-time | Hybrid
If you’re passionate about changing lives for the better, this is the opportunity you’ve been waiting for. In **Research & Development**, we’re continuously exploring innovative new treatment options to make a stronger, more positive impact on the lives of the patients we serve. You’ll work with talented colleagues in a state-of-the-art Research & Development environment, developing innovative medicines that change the life of patients for the better and help us make progress towards our vision of a world free of pain. Join us today, and discover the difference you can make.
**What the job looks like**
Each day you'll enjoy a variety of challenges, such as:
* You are responsible and accountable for developing and maintaining SDTMs, ADaMs, tables, figures and listings (TFL)
* You understand and review programming documents (e.g. SAP and mock TFLs, programming specifications, define and aCRF)
* You develop, document, validate and maintain SAS programs/macros for study requests
* You plan and participate in validation programming/QC activities of analysis outputs from external providers
* You support the development of data repositories, pooling of multiple studies for data mining purposes
* You support the development of data visualization and exploration tools and utilities as well as the development of programs for modeling and simulation activities
**What you'll bring to the table**
To make the most of this role and truly thrive, you should have:
* A Bachelor’s or Master’s Degree in Computer Science, Mathematics, Statistics or a related quantitative/ analytical field
* At least 5 years experience in SAS programming in clinical studies in the pharmaceutical industry including experience programming datasets and Tables/Figures/Listings utilizing CDISC standards
* Advanced proficiency in SAS programming and knowledge of other programming languages like R or Python is a plus
* Basic understanding of statistical methods commonly used in pharmaceutical clinical trials
* Thorough knowledge of and experience with CDISC standards
* Knowledge of ICH-GCP and other applicable legislation, with good understanding of clinical data and pharmaceutical development.
* You bring experience in a highly outsourced working environment collaborating with external service providers to ensures quality and timely deliverables.