Senior or Principal Clinical Data Scientist(m/w/x)

Ingelheim am Rhein, Biberach

VollzeitVor OrtSenior

Data Science

Jetzt bewerben

Nejo KI-Zusammenfassung

Planning and executing clinical pharmacology trials, including SRD/MRD and bioequivalence studies. Several years of drug development experience required. Hybrid setup with 1-2 days on site.

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Anforderungen

MSc in Statistics or Mathematics or comparable
Several years experience in drug development
Sound knowledge of statistical methodology
Knowledge of clinical pharmacology trial design
Basic medical terminology knowledge
Knowledge of clinical trial information processing
Advanced knowledge of SAS
Hands-on experience in SAS
Advanced knowledge of R
Hands-on experience in R
Familiarity with CDISC submission standards
Familiarity with FDA guidelines
Familiarity with EMA guidelines
Familiarity with regulatory requirements for clinical data analysis
Proactive issue identification
Proactive solution identification
Interaction with internal bodies on data science issues
Interaction with external bodies on data science issues
Strong interpersonal skills
Effective collaboration within organization
Effective collaboration outside organization
"We" mindset
Empathy
Trust-building skills
Curiosity
Big picture mindset
Oral communication skills
Written communication skills
Interaction in interdisciplinary teams
Ability to explain statistical information to non-statisticians
Ability to visualize statistical information for non-statisticians
Ability to communicate statistical information to non-statisticians
Fluency in written English
Fluency in spoken English
Doctoral Degree (PhD) with relevant professional experience
Master’s degree with longstanding relevant professional experience
Broad knowledge of complex clinical pharmacology trial designs
Advanced experience in complex clinical pharmacology trial designs
Broad knowledge of trial development processes
Advanced experience in trial development processes
Broad knowledge of corresponding data analyses
Advanced experience in corresponding data analyses
In-depth understanding of advanced statistical concepts
Understanding of statistical concepts relevant to clinical pharmacology trials
Severe disabilities are welcomed
Preferential consideration for equally qualified severely disabled applicants

Aufgaben

Plan and execute clinical pharmacology trials
Conduct first in human SRD/MRD studies
Perform bioequivalence and bioavailability studies
Analyze special populations and drug–drug interactions
Evaluate hADME and TQT studies
Develop statistical study designs and analysis plans
Provide analytical tools and outputs for high-quality trials
Apply established statistical methodologies
Integrate innovative data science approaches
Generate insights from clinical data
Collaborate with colleagues across disciplines
Enhance business and scientific expertise
Engage with the statistical and data science community
Lead and oversee complex clinical pharmacology trials
Guide colleagues and partners on statistics and data science

Berufserfahrung

ca. 4 - 6 Jahre

Ausbildung

Master-Abschluss

Sprachen

Englisch – fließend

Tools & Technologien

SASRCDISCFDAEMA

Benefits

Flexibles Arbeiten

Hybrid setup
1-2 days per week on site

Sonstige Vorteile

Global drug development environment

Von Nejo automatisch aufbereitet

Nejo hat diesen Job automatisch von der Website des Unternehmens Boehringer Ingelheim 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.

Zur Originalanzeige bei Boehringer Ingelheim

Über das Unternehmen

PharmaceuticalsIngelheim am Rhein

The company is focused on delivering lasting value to patients through innovative therapies and early clinical development.

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