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Job Post Details

Associate Specialist Biostatistics - job post

Nestlé
4.3/5 étoiles
Lausanne, VD
CDI, 100%
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Détails de l'emploi

Type de poste

  • CDI
  • 100%

Lieu

Lausanne, VD

Description du poste

Clinical Research Unit


Position Snapshot


Location: Nestlé Research, Lausanne, Switzerland
Institute: Clinical Research Unit
Company: Société des Produits Nestlé S.A.
Act. Rate: Full-Time Act. Rate 100%
Type of contract: Permanent contract


Important Information
: After submitting your application, you will be automatically invited to record a video introduction guided by specific questions. This video introduction should take no longer than 10 minutes. Once this step is completed, we would be pleased to consider your application and assess your profile accordingly. Kindly be informed that we will only consider candidates who have completed this step within 7 days from application. In case you miss this step, we will regretfully conclude that you are withdrawing your application.


What we offer at Nestlé


Genuine opportunities for career and personal development
Modern “smart office” locations providing agile & collaborative workspaces
Dynamic international working environment
Attractive additional benefits
Discover the true essence of Nestlé Research and watch our insightful video, showcasing our values and commitment to fostering a fulfilling work environment.


Position Summary


We are looking for an Associate Specialist Biostatistician, to handle the statistical aspects of ongoing clinical trials.


Nestlé Research is based in Lausanne, Switzerland, employs approximately 1000 people and is comprised of five Nestlé Institutes: Food Sciences, Health Sciences, Food Safety & Analytical Sciences, Packaging Sciences, and Agricultural Sciences. Unlock the door of our organization and find out more about our research activities and expertise here.


A Day in the Life of an Associate Specialist Biostatistician


  • Program the statistical analyses of ongoing clinical trials
  • Present the trial results to the trial team and at the investigator meeting, helping in the interpretation of the results
  • Write the statistical section in the trial protocol, considering the design and the objectives of the trial under supervision of a more experienced team member
  • Write the statistical analysis plans in agreement with the protocol, ensuring compliance with current guidelines and internal processes under supervision of a more experienced team member
  • Contribute to the clinical trial risk assessment
  • Share within the team the lessons learned and organizes the knowledge management


What will make you successful


  • MSc or PhD degree in Statistics or similar domains
  • Post-graduation experience, possibly in an industry research setting is a plus
  • Knowledge of statistical programming with at least R or SAS (both is ideal).
  • Strong analytical and organizational skills
  • Good communication skills to scientists and non-scientific audiences
  • Interest in applying statistical knowledge to innovations in nutrition and health
  • Proficiency in English
  • Knowledge of industry standards and regulatory guidance in clinical research is a plus (e.g. GCP)
  • Knowledge of clinical trial designs is a plus


Nestlé is committed to the accessibility of its recruitment process. If you require an adaptation during the recruitment process, please do let us know so we can support you effectively. All information will be treated confidentially.


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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