Clinical Research Scientist

Ligence is a fast growing company working on the forefront of cardiovascular diagnostics. Our AI-powered software automates the review of echocardiography studies — transforming how cardiology is practiced. We’re not just building products; our aim is to make a lasting impact in the history of medicine.  To help us scale our clinical presence globally, we’re looking for a Clinical Research Scientist to join our mission and contribute to clinical studies with world-renowned hospitals. 📍 Location: Remote/Hybrid⏳ Commitment: 1. 0 FTE📜 Contract:

Open-ended (3-month trial period)What would your day look like?We move quickly—launching a new clinical study every 2–3 months: You would work together with our medical doctors in designing and initiating these trials. After confirming the clinical study protocol, you would lead the study in terms of communicating with the study site and ensuring the study initiation. Once study is ongoing you would review clinical data as it is collected, ensuring it meets quality standards.

You will also be responsible for the documentation of the clinical trial management, ensuring all records are accurate, up to date, and compliant with regulatory requirements. You will be supported by our team of engineers, medical doctors, data scientists and regulatory experts along the way. We work with some of the best known hospitals in the world so you will be on the bleeding edge of AI applications in medicine. Once data is gathered at the clinical site, you would be tasked with reviewing it and preparing a study report.

Finally, you would present the findings that contribute to regulatory submissions (such as FDA, CE). This is a remote-friendly position with flexibility, provided your schedule aligns with Central European Time (CET, 8 AM–8 PM). Occasional site visits may be required. Key ResponsibilitiesDesigning and leading clinical trials for diagnostic cardiovascular devices/software tools. Outreach to clinical partners in organizing and overseeing clinical study. Clinical data evaluation and report writing for medical device regulatory purposes. Documentation and maintenance of all aspects of clinical trial management, including study plans, protocols, communications, and compliance records. RequirementsMaster’s or PhD degree in a biomedical field.

1+ year work experience in industry clinical research (preferably healthcare or medtech startups)Experience in designing and conducting clinical studies, specificallyDefining study cohorts, inclusion and exclusion criteriaChoice of metrics and study success criteria for diagnostic devicesExperience in communicating with trial sites and physiciansExperience in writing clinical study reports and performing literature reviewBonus: Statistical analysis skills using Python or RTrack record of scientific publications Experience in medical device submissions to regulatoryWhy Join Us?🚀 Be part of an innovative AI-driven medical device company transforming echocardiography. 🌎 Work with a team of engineers, data scientists, and clinicians at the forefront of medical AI.

💡 Influence product development and clinical validation of innovative cardiology tools. 🌍 Hybrid remote work – work flexibly from home or our office. 🕒 Flexible hours to accommodate your workflow and productivity. 📈 Stock options – be rewarded for your contribution to our success. 🍏 Office snacks to keep you energized throughout the day. 💰 Gross salary: €2,800 – €5,500/month (1FTE) (negotiable, based on experience and competencies).