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R&D Master Intern(m/w/x)
Description
In this role, you will gain hands-on experience by performing clinical procedures and managing study data, ensuring every project meets strict regulatory standards and timelines.
Let AI find the perfect jobs for you!
Upload your CV and Nejo AI will find matching job offers for you.
Requirements
- •Enrollment or graduation in Nursing degree
- •Passion for clinical research
- •Strong analytical thinking
- •Organization and priority management skills
- •Experience in clinical projects as sub-investigator (plus)
- •Prior nursing experience in healthcare settings (plus)
- •Familiarity with data collection software (plus)
- •Fluency in English and French
Education
Tasks
- •Ensure research activities comply with local laws and GCP standards
- •Prepare regulatory documents and facilitate Ethical Committee submissions
- •Maintain the Investigator Site File and study materials
- •Implement recruitment strategies and enroll study participants
- •Coordinate and document daily participant tests and procedures
- •Collect and manage study data to ensure protocol accuracy
- •Participate in internal close-out meetings and archive documents
- •Screen potential participants and document medical histories
- •Perform biological sample collection and monitor safety surveillance
Tools & Technologies
Languages
English – Business Fluent
French – Business Fluent
Benefits
Career Advancement
- •Career development opportunities
Flexible Working
- •Flexible working arrangements
Informal Culture
- •Inclusive and international environment
Other Benefits
- •Recruitment process accessibility support
- SUSONITYFull-timeInternshipOn-siteCorsier-sur-Vevey
- SUSONITY
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R&D Master Intern(m/w/x)
The AI Job Search Engine
Description
In this role, you will gain hands-on experience by performing clinical procedures and managing study data, ensuring every project meets strict regulatory standards and timelines.
Let AI find the perfect jobs for you!
Upload your CV and Nejo AI will find matching job offers for you.
Requirements
- •Enrollment or graduation in Nursing degree
- •Passion for clinical research
- •Strong analytical thinking
- •Organization and priority management skills
- •Experience in clinical projects as sub-investigator (plus)
- •Prior nursing experience in healthcare settings (plus)
- •Familiarity with data collection software (plus)
- •Fluency in English and French
Education
Tasks
- •Ensure research activities comply with local laws and GCP standards
- •Prepare regulatory documents and facilitate Ethical Committee submissions
- •Maintain the Investigator Site File and study materials
- •Implement recruitment strategies and enroll study participants
- •Coordinate and document daily participant tests and procedures
- •Collect and manage study data to ensure protocol accuracy
- •Participate in internal close-out meetings and archive documents
- •Screen potential participants and document medical histories
- •Perform biological sample collection and monitor safety surveillance
Tools & Technologies
Languages
English – Business Fluent
French – Business Fluent
Benefits
Career Advancement
- •Career development opportunities
Flexible Working
- •Flexible working arrangements
Informal Culture
- •Inclusive and international environment
Other Benefits
- •Recruitment process accessibility support
About the Company
Société des Produits Nestlé S.A.
Industry
Food
Description
The company develops new products, processes, and packaging concepts for a broad range of Nutrition, Dairy, Health Science, and Coffee products.
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