Description
EndoSurge is a breakthrough med-tech startup based in Stuttgart, Germany, advancing the future of interventional medicine with remotely controlled, MRI-compatible robotic systems designed for radiation-free, image-guided cardiovascular procedures. We are committed to building next-generation medical technologies that make a real difference in patient care. Our diverse team—originating from the Max Planck Institute for Intelligent Systems—brings together deep expertise in robotics, engineering, and medical imaging to address the growing challenges faced by today's healthcare providers.
EndoSurge is reimagining minimally invasive surgery by combining precision robotics, magnetic actuation, and real-time MRI guidance. Our mission is to create safer, more accurate, and more accessible interventions—eliminating radiation exposure and enabling clinicians with intuitive control systems and AI-assisted navigation. Join us at the forefront of medical robotics, artificial intelligence, and advanced imaging to help shape the next era of patient-centered care.
Responsibilities
As a Clinical Translation Scientist,
you will lead the design and execution of preclinical strategies to ensure the safe and effective delivery of robotic surgical systems towards first inhuman studies. You will contribute to the execution of preclinical studies, draft and review regulatory documents for both the FDA and Notified Bodies, coordinate with external investigators and CROs, and plan first inhuman studies. This position requires a strong foundation in the ability to analyze preclinical literature, interpret data, and communicate preclinical findings and evidence strategies to internal and external stakeholders, including regulatory bodies.
Required Qualifications
· Bachelor's degree in Clinical Research or related field
· years of experience in clinical research or clinical science in a medical device, pharma, or academic setting (or 2+ years with a Master's/PhD)
· Knowledge of
ISO 13485
,
ISO 14155
,
IEC 60601
, and
ISO 14971
standards
· Knowledge of
phantom studies
,
pre-clinical animal models
, or
in vivo validation
· Ability to analyze clinical data and interpret peer-reviewed literature to support evidence generation
· Excellent oral and written communication skills in English
Preferred Qualifications
· Masters', MD, or PhD Degree in Clinical Research or related field
· Certification or training in Good Clinical Practice (GCP) and Clinical Research Regulations (FDA, EMA, ISO 14155)
· Experience designing and conducting clinical studies, pilot trial design, or post-market clinical follow-ups (PMCF)
· Knowledge of FDA, EMA, and Notified Body requirements for medical device approval
· Knowledge of clinical evaluation reports (CERs) and regulatory documentation
· Excellent oral and written communication skills in German
What We Offer
Employees are eligible for the following benefits listed below:
· You will receive a fixed-term employment contract according to TVöD (public sector employment). The duration depends on your qualification goals.
· Childcare facilities and equal opportunity offers to support work-life balance
· Access to Max Planck career coaching and German language training courses
· Consideration for employee stock options
· Assistance in relocation from abroad
Application Requirements:
· CV
· Cover letter
· Contact info of two references