(Associate) Scientist Clinical Biostatistics

vor 24 Stunden

Stuttgart, Deutschland Immatics Biotechnologies GmbH Vollzeit

**Overview**:
We are currently seeking a full-time
**(Associate) Scientist Clinical Biostatistics/ Statistical Programming**. You will work in Tübingen, in Munich or remote (Germany). As part of our Translational Science Team you’re in close contact with our clinical departments as well as various other departments across the Company. Initial experience or deep interest in handling of clinical trial data and clinical biostatistics/ statistical programming is necessary. More in-depth skills can be acquired quickly with the support of our experienced colleagues and a suitable individual training plan.

**Your mission**:
Your main responsibilities will include but are not limited to the following tasks:

- Reporting of safety data
- Contribute to writing of clinical and regulatory study documents
- Answer translational/ exploratory questions
- Contribute to publication of clinical trial data
- Provide support across all statistical tasks during the lifecycle of our programs, including clinical study protocol design, statistical analysis plan (SAP) development and the preparation of interim data readouts and finally the clinical study report.
- Support the accurate and complete data collection in the clinical EDC systems in close collaboration with the data management team.
- Oversee accurate completion of biostatistical outputs (SDTM, ADaM, TFLs) generated by external vendors, ensuring that the expected standards are met and that the outputs are in line with the analyses described in the SAP.
- Contribute to improving data analysis workflows, as well as implementing and executing quality measures to ensure data integrity, in close collaboration with the clinical teams.

**Your profile**:

- You hold a master’s degree or PhD in life sciences or biostatistics, ideally with a focus in clinical biostatistics and/ or statistical programming.
- First industry experience in analysis and reporting of clinical trial data is a plus.
- You exhibit a great attention to detail with strong affinity to answer scientific questions.
- Insights into programming in SAS, R, SQL and good programming practice are an advantage.
- Ideally, you worked already with eCRFs and JReview and gained knowledge of applicable clinical research regulatory requirements (i.e., GCP, ICH guidelines).
- We expect a high degree of independent working, analytical reasoning, and good communication skills in English.
- Basic knowledge in immunology, oncology and/ or cell and gene therapy would be an advantage.

**Why us?**:
We are a committed and inspired team and cherish the collegial, highly motivated, and family-friendly atmosphere within Immatics. Our culture allows for a high level of originality, independent thinking, and initiative. We believe in supporting our employees’ professional and social skills: We enable them to join conferences and trainings as well as to enjoy our Immatics benefits - e.g., job bike, job ticket, Health Programs, childcare benefits, relocation allowance, Company summer and winter events.

**Notice**:

- We value diversity and inclusion. Immatics N.V. and all Immatics subsidiaries are equal opportunity employers that evaluate qualified applicants without regard to race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law.

**About us**:

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