Research Assistant Data Management

vor 1 Tag

Lausanne, Schweiz Nestle Vollzeit

**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

**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

**Position Summary**

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

As
**Research Assistant Data Management**, you will be responsible for developing and implementing the strategy for managing the trial data on all assigned clinical studies. You will manage all activities covering the data management process including data base set-up, remote monitoring and data base lock.

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 a Research Assistant Data Management**
- Provide clinical data management support to clinical projects
- Review and update clinical study documents (e.g., protocols)
- Set up the clinical database, including consistency checks defined in the Data Validation Plan
- Develop Data Transfer Agreement with external data vendors and/or core labs
- Coordinate the clinical data quality review during the study execution
- Collaborate with Biostatisticians on data validation and lock of the database, including management of discrepancies
- Prepare and maintain key documents for the data management activities in a trial
- Collaborate with cross-functional internal resources (biostatistician, clinical project manager, scientists, medical directors) on different health benefit areas

**What will make you successful**
- MSc degree with a scientific background
- At least 5 years’ experience in the field of clinical research
- Up to date on regulations regarding clinical data collection and on clinical data standards such as: GCP (Good Clinical Practice), GCDMP (Good Clinical Data Management Practices), data privacy, and new regulations like GDPR (General Data Protection Regulation)
- Knowledge and interest in digital transformation tools contributing towards data management will be advantageous
- Experience with Data Management Systems such as Medidata
- Project management skills
- Central monitoring and analytical skills are advantageous
- Problem solving skills with a desire to improve current processes
- Ability to ‘think outside of the box’
- Excellent communication skills, both oral and written 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.

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