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 ...