Biostatisticians

☞ Make A Healthy Change

View: 208

Update day: 26-03-2024

Location: Lausanne Vaud VD

Category: R & D Quality Assurance / Quality Control Other

Industry: Consumer Goods Food & Beverages Food Production

Job type: Full-time

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Job content

Position Snapshot

Location: Nestlé Research, Lausanne, Switzerland

Company: Société des Produits Nestlé S.A.

Act. Rate: Full-Time Act. Rate 100%

Type of contract: Permanent contract

MSc or PhD degree in Biostatistics

Genuine opportunities for career and personal development

Modern “smart office” locations providing agile & collaborative workspaces

Dynamic international working environment

Position Summary

Attractive additional benefits

Nestlé Research is based in Lausanne, Switzerland, employs approximately 1000 people and is comprised of four Nestlé Institutes: Material Sciences; Health Sciences, Food Safety & Analytical Sciences and Packaging Sciences. Please have a tour of our facilities using this link or read more about Nestlé Research at our website.

The Biostatistician is responsible for all statistical tasks of individual clinical trials. Your main responsibility will be to suggest and prepare optimal statistical designs, provide statistical inputs into the design of protocols including preparation of the statistical analysis plan, analyze and report results of clinical trials.

We offer a dynamic, inclusive, and international working environment with many opportunities across different companies, functions, and regions. Don’t miss the opportunity to join us and work with different teams in an agile and diverse context.

A day in the life of Biostatistician
  • Contribute to the scientific substantiation of the benefits of Nestlé products and knowledge building in nutrition
  • Judge scientific background knowledge and assess risks
  • Understand business relevance, know clinical trial designs, state practical and valid statistical hypothesis
  • Suggest sound statistical analyses, review clinical trial synopsis
  • Understand the clinical trial process, guidelines and statistics
  • Write statistical analysis plans which are in agreement with the protocol, feasible, understandable for non-statisticians, efficient, valid and respecting guidelines (GCP)
  • Perform programming in one statistical programming environments
  • Communicate with business and all stakeholders of the clinical trial
  • Present the results at the investigator meeting

What Will Make You Successful
  • MSc or PhD degree degree in Biostatistics
  • Knowledge in CONSORT-statement, past experience with the peer-review system
  • Excellent level of statistical programming
  • Strong analytical and organizational skills
  • Understanding of scientific principles and business needs
  • Good communication skills with scientific and business partners
  • Knowledge of GCP-guidelines and understanding of the rationale behind these
  • Experience in clinical trial designs
  • Good in written and oral communication in English

At Nestlé, we want to help shape a better and healthier world, inspire people to live healthier lives and deliver impact at a scale and pace that makes a difference. We do this by fostering a diverse, friendly, supportive, and collaborative environment, that creates positive disruption, embraces innovation, and empowers people and teams to win.

We aim to hire friendly, respectful, inspiring people who care about the people’s lives that we touch every single day.

Be a force for good. Join Nestlé and visit us on www.nestle.com.
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Deadline: 10-05-2024

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