Biostatistician

2 months ago

Bengaluru Karnataka, India Merck KGaA Full time

Work Your Magic with us

Ready to explore, break barriers, and discover more? We know you've got big plans '“ so do we Our colleagues across the globe love innovating with science and technology to enrich people's lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us.

United As One for Patients, our purpose in Healthcare is to help create, improve and prolong lives. We develop medicines, intelligent devices and innovative technologies in therapeutic areas such as Oncology, Neurology and Fertility. Our teams work together across 6 continents with passion and relentless curiosity in order to help patients at every stage of life. Joining our Healthcare team is becoming part of a diverse, inclusive and flexible working culture, presenting great opportunities for personal development and career advancement across the globe.

As a study biostatistician for statistically standard clinical studies and under supervision:

- perform statistical analyses or validate statistical output as required or able to conduct oversight of vendor for these studies
- write comprehensive statistical methods sections for the clinical study report; critically review and coauthor these reports ensuring the accuracy of the statistical interpretation.
With surpervision, able to effectively perform ad'hoc analysis or project related standard reporting (e.g., DSUR)
Understand and follow all Global Biostatistics WIs/SOP and relevant Standards as well as any other relevant WIs/SOPs.

May act as an interface between programming and statistic. The responsibilities include but are not limited to performing complex statistical analyses. With expertise in statistics and programming you be able to transform complex statistical models into programming code and use state-of-the-art modelling techniques to provide solutions. Further, will supervise CROs and provide advice and technical solutions on programming task and standard macros. Will closely work with the project statisticians and project programmers in addition to clinical and project teams.

Requirement:
'¢ MS in Statistics, Biostatistics or related discipline
'¢ Fluent in English (written and spoken)

**Skills**:'¢ SAS and R practical and effective knowledge
'¢ Ability to develop an understanding of relevant clinical therapeutic areas
'¢ Results driven
'¢ Collaborative
'¢ Act purposefully

**What we offer**:We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We celebrate all dimensions of diversity and believe that it drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress

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