In your first months, you’ll focus on:

• Coordinating clinical trials in accordance with Good Clinical Practice and ISO 14155:2020, including trial monitoring ensuring high quality data
• Working closely with trial sites and principal investigators
• Designing clinical studies for technology development purposes together with the engineering team
• Analyzing and reporting clinical study results
• Supporting the reporting to the ethics committee and Notified Body
• Leading biomedical working students to perform study-related projects (such as data annotation)
• Other tasks including but not limited to providing demos to customers, supporting the engineering team with bench tests, literature research

This is what your success looks like
After 12 months you are the go-to person for coordinating clinical trials required for technology, regulatory and scientific purposes. You have established strong relationships with principal investigators at the trial sites.

• Master’s degree in Health or Life Sciences (e.g., Medicine, Technical Medicine, Public Health, Pharmaceutical Sciences, Biomedical Sciences, or related)
• 0-2 years of working experience
• Strong organizational skills
• Excellent (written/verbal) communication skills in Dutch and English
• Preferably data analysis experience (e.g., Python, R) and knowledge of biostatistics
• Preferably experience with Good Clinical Practice
• Full-time availability, with at least 3 days per week onsite in Utrecht
• Willingness to travel to trial sites in Amsterdam, Utrecht, Dordrecht

Founded in 2017 in Utrecht, Vitestro is pioneering the future of blood collection with the Aletta® Autonomous Robotic Phlebotomy Device™ (ARPD™). This groundbreaking medical device combines advanced multimodal imaging (near-infrared, ultrasound, and Doppler ultrasound) with robotics and AI to perform the entire diagnostic blood draw procedure autonomously.

By addressing critical healthcare staffing shortages and improving patient experience, Vitestro is transforming one of the most common and essential medical procedures. With more than 90 team members and growing rapidly, we are scaling our impact. As we placed our first devices with customers, we are now expanding our team to ensure successful implementation and long-term reliability.

At Vitestro, we are committed to continuous innovation and improvement.

• Competitive salary including pension plan
• 25 days of annual leave based on a full-time position
• Hybrid work model
• Working together in a high-skilled team with our home base in Utrecht
• Frequent out-of-work activities with our team, and annual company weekend away
• Annual training budget of €2000,-
• Opportunity to be key shaper of a new global industry niche: autonomous medical robotics

Vitestro offers an environment where you can make a lot of impact, as you are joining a growing scale-up in MedTech. The team of driven and talented colleagues enjoys solving the challenges in developing, manufacturing, and completing our breakthrough medical device. While working in an open culture, they strive for excellence in all domains. And believe in taking courage and like to challenge each other. They learn and teach, regardless of age, nationality or gender.