Clinical Study Intern

greenteg AG

Intern aiding in clinical research at Hospital of Lucerne for greenteg AG. Focused on data collection, patient recruitment, and study protocol adherence.

Posted 7/17/2026internshipRümlang • 🇨🇭 SwitzerlandEntry LevelWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in data collection and management within clinical research settings, with a strong emphasis on patient interaction, ethical standards, and physiological research methods. Proficient in both German and English, ensuring effective communication in a diverse environment.

Highest-signal resume keywords

Data CollectionPatient RecruitmentGood Clinical Practice (GCP)Physiological Research MethodsData Management

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Data CollectionData ManagementBasic Data Quality ChecksLiterature ResearchStudy Protocols

Soft Skills

Interpersonal SkillsCommunication SkillsIndependenceResponsibility

Tools & Technologies

Study Equipment

Certifications & Qualifications

GCP (Good Clinical Practice) TrainingValid Swiss Work Permit

Industry Keywords

Health SciencesPhysiologyPatient ConfidentialityResearch EthicsFever PhysiologyCore Body Temperature Measurement

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Support data collection at Lucerne Hospital during a six-month internship
Recruit patients for the study
Collect data according to the study protocol (e.g., obtaining informed consent, instructing participants, applying sensors, and conducting regular check-ins)
Perform data management and basic data quality checks
Organize and maintain study equipment
Conduct literature research related to fever physiology and core body temperature measurement

Requirements

What you’ll need

Bachelor’s degree or higher in Health Sciences, Physiology, or a related medical field
Strong interpersonal and communication skills; comfortable approaching and interacting with patients
Basic knowledge of data protection, patient confidentiality, and research ethics; GCP (Good Clinical Practice) training is a plus
Familiarity with physiological research methods and study protocols
Ability to work independently and take responsibility
Proficiency in German and English (written and spoken)
Valid Swiss work permit
Available to work on-site at Lucerne Hospital, Switzerland
Working days: Monday to Friday

Benefits

Comp & perks

Hands-on experience working on a clinical study in a hospital setting
Insight into the R&D activities of a wearable technology company