Internship Master 2: Clinical Research, HealthTech & AI

At echOpen factory, we are at the forefront of healthcare technology, developing a revolutionary ultra-portable, tri-frequency ultrasound imaging probe that connects to any smartphone or tablet, announced as the the “21st-century stethoscope.
This internship is uniquely positioned at the intersection of clinical research, quality control, regulatory compliance, and AI research and development, encompassing both software and hardware perspectives. It offers a rich learning experience in a dynamic field, blending various complex subjects. As an intern here, you will contribute significantly to health improvement initiatives and enjoy a multifaceted educational journey.


  • Planning and Monitoring Clinical Studies: Engage in different phases of clinical studies, including design, data analysis, and compilation of results, with a focus on AI technologies.
  • Participation in AI R&D: Assist in designing validation studies, defining state-of-the-art approaches, and overseeing the data pipeline, ensuring labeling accuracy, GDPR compliance, and robust cloud & cybersecurity measures.
  • Systematic Literature Reviews: Contribute to conducting and updating systematic literature reviews in accordance with PRISMA guidelines.
  • Regulatory Documentation Drafting: Participate in the preparation of key regulatory documents, including Clinical Investigation Plans and Reports, Clinical Evaluation Plans and Reports, and more.

Required Education:

  • Undergraduate degree (or equivalent) in a relevant field such as Biomedical Engineering, Clinical Research, Computer Science, Data Science, or related areas.

Essential Skills:

  • Clinical Research Acumen: Understanding of clinical study design, implementation, and analysis.
  • AI and Machine Learning Knowledge: Familiarity with AI technologies and machine learning principles applicable to healthcare.
  • Communication Skills: Good written and verbal communication abilities for drafting reports and presenting research findings.
  • Problem-Solving: Good analytical and problem-solving mindset, with the ability to work independently and as part of a team.

Desirable Experience:

  • Systematic Literature Review Skills: Experience in conducting literature reviews following established protocols like PRISMA

Personal Attributes:

  • Highly motivated and committed to the advancement of healthcare technology.
  • Eagerness to learn and adapt in a fast-paced, interdisciplinary environment.
  • Good organizational skills.

Supervision: Supervision will be provided by a medical practionner (MD, PhD) with a soifd background in Clinical Research. Training sessions will be held as an introduction to clinical research regulatory framework for medical devices, with a special focus on AI.

Duration of employment: 6 months

Starting date: Asap

Location: Full-time position based at the Hôtel Dieu hospital (Paris 4th).

Salary: Dependent on the profile and experience of the candidate

Team contact and application details: +33650332892

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