Job Description

We are searching intelligent and innovative employees. If you are interested in working for a dynamic company with flat hierarchy, we look forward to receiving your application.


Your tasks:

Database Setup (IDB):

Planning, execution, and quality control of statistical and programming activities for the integration of clinical databases.

Statistical Analyses:

Design, execution, and oversight of statistical analyses for individual clinical studies and integrated datasets.

Study Planning:

Providing statistical input for clinical development programs, study protocols, and regulatory documents (e.g., CTDs).

Meta-Analyses:

Conducting meta-analyses for effectiveness comparisons with competitor products.

Cross-Functional Collaboration:

Advising internal R&D teams on statistical topics and interpretation of results.

Publications:

Contributing to and reviewing scientific publications and presenting statistical results.

Regulatory Interactions:

Coordinating and discussing statistical aspects with regulatory authorities.

Process Optimization:

Continuously improving biostatistics processes to meet evolving regulatory and organizational requirements.
Your profile:


Graduate studies in Statistics, Mathematics, Epidemiology, Computer or Data Sciences At least 3 years experience in Biostatistics Experience with SAS, CDISC, ICH, GCP, FDA guidelines Experience with intergrated databases and EDC systems Fluent English skills, German is a plus
You can expect ...


Experience in exciting and international projects Continuous salary development Da Vinci Corporate Benefits On-the-job training and language courses Appreciation, motivation and commitment

Nothing provides more motivation than success. Da Vinci Engineering is highly committed to ensuring the own employees' success. Become a part of us!


Nicht zögern. Gleich bewerben!



Frau Andrea CindricDa Vinci Engineering GmbHHauptstätter Straße 14970178 Stuttgart+49 711 72240 107

job@davinci.de