Senior or Principal Statistician - Remote/Hybrid

3w3 weeks ago

Boehringer Ingelheim

Biberach an der Riß, DE · Full-time · €90,000 – €130,000

About this role

Join a team where your expertise drives meaningful scientific progress in Global Experimental Medicine. We drive forward innovative therapeutic concepts and drug candidates that offer clear benefits for patients, striving to achieve early patient proof of concepts with speed and precision.

In this role, you will be responsible for the planning and execution of clinical pharmacology trials such as first-in-human SRD/MRD, bioequivalence, bioavailability, and drug-drug interaction studies. You will oversee all aspects of data analytics, developing statistical study designs and analysis plans to support high-quality trial delivery.

Working closely with colleagues from various disciplines across Experimental Medicine, you will provide statistical expertise and integrate innovative data science approaches to generate insights. You will also exchange knowledge with the statistical and data science community inside and outside of Boehringer Ingelheim.

This position offers the chance to enhance your business knowledge and scientific expertise in a global drug development environment. As a Principal Statistician, you will additionally lead complex trial design, analysis, and reporting, guiding colleagues and partners on statistics and data science tasks.

Requirements

Master of Science (MSc) in Statistics or Mathematics or comparable with several years of experience in drug development.
Sound knowledge of statistical methodology, design of clinical pharmacology trials, basic medical terminology, and processing clinical trial information.
Advanced knowledge of and hands-on experience in relevant software languages, like SAS and R.
Familiarity with submission standards such as CDISC, FDA, EMA guidelines and regulatory requirements for clinical data analysis.
Ability to proactively identify issues and solutions and to interact with internal and external bodies on routine data science issues.
Strong interpersonal skills for effective collaboration within and outside of the organization.

Responsibilities

Plan and execute clinical pharmacology trials such as first-in-human SRD/MRD, bioequivalence, bioavailability, special populations, drug-drug interaction, hADME, and TQT.
Oversee all aspects of data analytics, developing statistical study designs and statistical analysis plans, and provide analytical tools and outputs for high-quality trial delivery.
Apply established statistical methodologies and integrate innovative data science approaches to design studies and analyze clinical data from clinical pharmacology trials.
Work closely with colleagues from various disciplines across Experimental Medicine and Medicine, providing statistical expertise to support clinical pharmacology trials.
Exchange with the statistical and data science community inside and outside of Boehringer Ingelheim to enhance expertise.
Lead and oversee the design, analysis, and reporting of complex clinical pharmacology trials (additional for Principal positions).
Lead and guide colleagues as well as internal and external partners on statistics and data science-related tasks (additional for Principal positions).

Benefits

Hybrid work model with approximately 1-2 days per week on site.
Opportunity to shape the future of Experimental Medicine and early patient proof of concepts.
Collaboration with a global statistical and data science community inside and outside the company.
Support for innovative data science approaches in a global drug development environment.