Immatics Biotechnologies GmbH
Medical Monitor*(m/w/x)
Vollzeit/Teilzeitmit HomeofficeBerufserfahren
Tübingen, München
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IMImmatics Biotechnologies GmbH
(Senior) Clinical Statistical Programmer – SAS*(m/w/x)
Tübingen, München
Vollzeitmit HomeofficeBerufserfahren
Data Science
Nejo KI-Zusammenfassung
Developing and validating CDISC compliant SDTM/ADaM datasets for cancer immunotherapy clinical studies at a biotech firm. Strong SAS proficiency in clinical research and 3-5 years industry experience required. Job bike, job ticket, childcare benefits, relocation allowance.
Anforderungen
- Bachelor’s or Master’s degree in statistics, data science, life sciences, or related field
- Strong proficiency in SAS in a clinical research setting
- Experience in R
- Minimum 3-5 years of industry experience as a statistical programmer
- Familiarity with clinical research regulations such as GCP and ICH guidelines
- Strong attention to detail
- Highly structured and methodical working style
- Ability to work independently
- Analytical thinking
- Clear and effective communication in English
- German language skills
- Basic knowledge of immunology, oncology, and/or cell and gene therapy
Aufgaben
- Collaborate with biostatisticians to develop, validate, and review Tables, Figures, and Listings (TFLs) for clinical studies
- Clarify data specifications and address data quality issues with biostatisticians and data managers
- Ensure timely and accurate delivery of statistical outputs in line with protocol requirements and project timelines
- Support programming implementation of Statistical Analysis Plans, including mock TFLs and derived datasets
- Assist in the development, review, and validation of CDISC compliant SDTM and ADaM datasets
- Participate in documentation, TMF filing, and compliance activities following Good Clinical Practice (GCP) and ICH guidelines
- Contribute to the preparation and quality control of statistical outputs, regulatory submission packages, and Clinical Study Reports
- Identify opportunities for greater efficiency and standardization in data analysis workflows
- Develop and apply quality control measures to ensure integrity, reproducibility, and regulatory compliance of statistical programming outputs
Berufserfahrung
- 3 - 5 Jahre
Ausbildung
- Laufendes StudiumODER
- Bachelor-AbschlussODER
- Master-Abschluss
Sprachen
- Englisch – verhandlungssicher
- Deutsch – Grundkenntnisse
Tools & Technologien
- SAS
- R
Benefits
Firmenfahrrad
- Job bike
Öffi Tickets
- Job ticket
Gesundheits- & Fitnessangebote
- Health programs
Kinderbetreuung
- Childcare benefits
Sonstige Zulagen
- Relocation allowance
Team Events & Ausflüge
- Company summer events
- Company winter events
Die Originalanzeige dieses Stellenangebotes in der aktuellsten Version findest du hier. Nejo hat diesen Job automatisch von der Website des Unternehmens Immatics Biotechnologies GmbH 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.
Noch nicht perfekt?
- Immatics Biotechnologies GmbH
Director Clinical Sciences(m/w/x)
Vollzeit/Teilzeitmit HomeofficeManagementTübingen, München - Immatics Biotechnologies GmbH
Medical Monitor*(m/w/x)
Vollzeit/Teilzeitmit HomeofficeBerufserfahrenTübingen, München, Berlin - Immatics Biotechnologies GmbH
GCP/ GCLP Auditor as Senior Manager Clinical Quality Assurance(m/w/x)
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Senior Data Engineer(m/w/x)
Vollzeitmit HomeofficeSeniorDüsseldorf, Stuttgart, Fürth, Hamburg, Berlin, Essen, Frankfurt am Main, München, Tübingen
IMImmatics Biotechnologies GmbH
(Senior) Clinical Statistical Programmer – SAS*(m/w/x)
Tübingen, München
Vollzeitmit HomeofficeBerufserfahren
Data Science
Nejo KI-Zusammenfassung
Developing and validating CDISC compliant SDTM/ADaM datasets for cancer immunotherapy clinical studies at a biotech firm. Strong SAS proficiency in clinical research and 3-5 years industry experience required. Job bike, job ticket, childcare benefits, relocation allowance.
Anforderungen
- Bachelor’s or Master’s degree in statistics, data science, life sciences, or related field
- Strong proficiency in SAS in a clinical research setting
- Experience in R
- Minimum 3-5 years of industry experience as a statistical programmer
- Familiarity with clinical research regulations such as GCP and ICH guidelines
- Strong attention to detail
- Highly structured and methodical working style
- Ability to work independently
- Analytical thinking
- Clear and effective communication in English
- German language skills
- Basic knowledge of immunology, oncology, and/or cell and gene therapy
Aufgaben
- Collaborate with biostatisticians to develop, validate, and review Tables, Figures, and Listings (TFLs) for clinical studies
- Clarify data specifications and address data quality issues with biostatisticians and data managers
- Ensure timely and accurate delivery of statistical outputs in line with protocol requirements and project timelines
- Support programming implementation of Statistical Analysis Plans, including mock TFLs and derived datasets
- Assist in the development, review, and validation of CDISC compliant SDTM and ADaM datasets
- Participate in documentation, TMF filing, and compliance activities following Good Clinical Practice (GCP) and ICH guidelines
- Contribute to the preparation and quality control of statistical outputs, regulatory submission packages, and Clinical Study Reports
- Identify opportunities for greater efficiency and standardization in data analysis workflows
- Develop and apply quality control measures to ensure integrity, reproducibility, and regulatory compliance of statistical programming outputs
Berufserfahrung
- 3 - 5 Jahre
Ausbildung
- Laufendes StudiumODER
- Bachelor-AbschlussODER
- Master-Abschluss
Sprachen
- Englisch – verhandlungssicher
- Deutsch – Grundkenntnisse
Tools & Technologien
- SAS
- R
Benefits
Firmenfahrrad
- Job bike
Öffi Tickets
- Job ticket
Gesundheits- & Fitnessangebote
- Health programs
Kinderbetreuung
- Childcare benefits
Sonstige Zulagen
- Relocation allowance
Team Events & Ausflüge
- Company summer events
- Company winter events
Die Originalanzeige dieses Stellenangebotes in der aktuellsten Version findest du hier. Nejo hat diesen Job automatisch von der Website des Unternehmens Immatics Biotechnologies GmbH 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.
Über das Unternehmen
Immatics Biotechnologies GmbH
Branche
Healthcare
Beschreibung
The company combines the discovery of true targets for cancer immunotherapies with the development of T cell receptors to enable robust T cell responses against cancer.
Noch nicht perfekt?
- Immatics Biotechnologies GmbH
Medical Monitor*(m/w/x)
Vollzeit/Teilzeitmit HomeofficeBerufserfahrenTübingen, München - Immatics Biotechnologies GmbH
Director Clinical Sciences(m/w/x)
Vollzeit/Teilzeitmit HomeofficeManagementTübingen, München - Immatics Biotechnologies GmbH
Medical Monitor*(m/w/x)
Vollzeit/Teilzeitmit HomeofficeBerufserfahrenTübingen, München, Berlin - Immatics Biotechnologies GmbH
GCP/ GCLP Auditor as Senior Manager Clinical Quality Assurance(m/w/x)
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Senior Data Engineer(m/w/x)
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