(Senior) Biostatistician (m/f/d)

at  Da Vinci Engineering GmbH

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:

• Specification, conduct or coordination and quality control of statistical and programming activities for integration of clinical databases
• Statistical input to clinical development programs and clinical trials / investigations, including Clinical Development Plans, CTDs, etc.
• Meta-analyses for effectiveness comparisons vs. competitor’s products
• Interactions with other R&D functions including consultation on statistical topics and interpretation of results
• Coordination and discussion of all statistical aspects in interactions with regulatory bodies
• Ongoing optimization and actualization of biostatistics processes to reflect possible changes in regulatory and organizational requirements
• Specification, conduct or coordination and quality control of statistical analysis activities for individual studies and integrated analyses

Your profile:

• Graduate studies in Statistics, Mathematics, Epidemiology, Computer or Data Sciences
• At least 3 years experience in Biostatistics
• Fluent English, written and spoken
• Required experience with SAS, CDISC, ICH, GCP, FDA guidelines
• Preferable experience with Integrated databases and EDC systems
• High sense of resposibility and quality awareness
• Excellent organizational skills

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!

• Specification, conduct or coordination and quality control of statistical and programming activities for integration of clinical databases
• Statistical input to clinical development programs and clinical trials / investigations, including Clinical Development Plans, CTDs, etc.
• Meta-analyses for effectiveness comparisons vs. competitor’s products
• Interactions with other R&D functions including consultation on statistical topics and interpretation of results
• Coordination and discussion of all statistical aspects in interactions with regulatory bodies
• Ongoing optimization and actualization of biostatistics processes to reflect possible changes in regulatory and organizational requirements
• Specification, conduct or coordination and quality control of statistical analysis activities for individual studies and integrated analyse