Senior Biostatistician (m/f/d) in Bremen

GCP-Service International Ltd. & Co.KG; Bremen; Vor Ort; EUR 60.000 - 80.000; Vollzeit

Zusammenfassung

A leading clinical research organization in Bremen is expanding its team and seeking a full-time Senior Biostatistician. This role involves managing statistical aspects of clinical trials, including collaboration with sponsors and statistical analysis. Ideal candidates possess a Master's or PhD in Statistics/Biostatistics, have 3+ years of clinical research experience, and demonstrate excellent communication skills in English. This position offers an engaging environment with opportunities for personal and professional development.

Leistungen

Excellent working environment near the University of Bremen

Opportunities for personal development

Modern remuneration systems

Qualifikationen

• 3+ years of experience as Biostatistician in clinical research (CRO or Sponsor) is a strong plus, must-have for those without a PhD.
• Excellent spoken and written English (German is a plus).

Aufgaben

• Manage all statistical aspects of clinical trials from consultation to analysis.
• Communicate with the Sponsor on all statistical questions.
• Represent statistical concepts clearly to clients.

Kenntnisse

Statistical analysis

Communication skills

Problem-solving

Self-management

SAS proficiency

Understanding of regulatory requirements

Ausbildung

Master’s degree (MSc.) or PhD in Statistics or Biostatistics

Tools

SAS

Jobbeschreibung

We are expanding our team and are looking for a dynamicfull time Senior Biostatisticianwho 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
• 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®

We offer

• An independent, diverse and interesting area of responsibilities and an excellent working environment in the immediate vicinity of the University of Bremen
• A young and innovative corporate culture and management, with a clear path to personal development and the opportunity to take responsibility not only within projects, but also within the company
• Support and advancement in individual personal and professional developmentActive shaping of work processes
• Modern and performance-oriented remuneration systems

Thank you for submitting your application. We truly appreciate your interest in joining our company.

Please note that the review process may take some time. If you are selected to move forward, we will contact you within two weeks. If you are not selected, please understand that we will not be sending additional updates.

In accordance with the application procedure (Art. 6 para. 1b GDPR), we will retain your application documents for a period of six months. After this time, your data will be securely deleted. You have the right to request access to, rectification, or deletion of your personal data, to restrict or object to its processing, and to request data portability.

If you have any questions regarding data protection, please contact our Data Protection Officer at [e-mail].

We wish you all the best in your job search.

Best regards,

HR team @ GCP-Service International

If we have piqued your interest, we look forward to receiving your application. Please address it as follows, stating your salary expectations and the earliest possible starting date: