Biostatistician

We are expanding our team and are looking for a dynamic full time Senior Biostatistician who wants to join a young and motivated group of Biostatisticians in our headquarter in Bremen , and who is open to taking responsibility for projects and fellow team members alike.

We are expanding our team and are looking for a dynamic full time Senior Biostatistician who wants to join a young and motivated group of Biostatisticians in our headquarter in Bremen , and who is open to taking responsibility for projects and fellow team members alike.

• The responsibility of a Senior Biostatistician is to manage all statistical aspects which occur in the frame of a clinical trial - from initial consultation regarding study concepts, to providing input into study protocols and writing SAPs, to conducting the analysis and summarizing the results. In this context, we are looking for a candidate who understand the importance of the following:
• Statistical aspects throughout the entire course of clinical trials including establishment of qualification control tools and coordination of study processes
• Taking responsibility for the communication with the Sponsor and your colleagues regarding all statistical (and sometimes non-statistical) questions within a project
• Mentoring junior colleagues regarding statistical questions
• Having the confidence to represent statistical concepts in front of clients and presenting key information in an understandable manner to non-statisticians
• Being able to think outside the box and finding creative solutions to statistical problems given limited resources
• The responsibility of a Senior Biostatistician is to manage all statistical aspects which occur in the frame of a clinical trial - from initial consultation regarding study concepts, to providing input into study protocols and writing SAPs, to conducting the analysis and summarizing the results. In this context, we are looking for a candidate who understand the importance of the following:
• Statistical aspects throughout the entire course of clinical trials including establishment of qualification control tools and coordination of study processes
• Taking responsibility for the communication with the Sponsor and your colleagues regarding all statistical (and sometimes non-statistical) questions within a project
• Mentoring junior colleagues regarding statistical questions
• Having the confidence to represent statistical concepts in front of clients and presenting key information in an understandable manner to non-statisticians
• Being able to think outside the box and finding creative solutions to statistical problems given limited resources

• Your profile:
• Master's degree (MSc.) or PhD in Statistics or Biostatistics
• 3+ experience as Biostatistician in clinical research (CRO or Sponsor) is a strong plus, and must-have for statisticians without PhD
• Excellent communication and self-management skills
• Excellent understanding of regulatory requirements of clinical trials, with a particular focus on statistical requirements
• Excellent spoken and writing English (German is a plus)
• Good command of SAS®
• Your profile:
• Master's degree (MSc.) or PhD in Statistics or Biostatistics
• 3+ experience as Biostatistician in clinical research (CRO or Sponsor) is a strong plus, and must-have for statisticians without PhD
• Excellent communication and self-management skills
• Excellent understanding of regulatory requirements of clinical trials, with a particular focus on statistical requirements
• Excellent spoken and writing English (German is a plus)
• Good command of SAS®