Project Engineer – Clinical Trial Configuration
Posted on March 23, 2026 (2 months ago)
This job post is archived - the company is no longer hiring for this position.
Check out other job posts of this company here!About Mint Medical
Mint Medical is a global MedTech company in the field of data-driven radiology and a pioneer of personalized medicine. We support radiologists by making radiological image data usable for interdisciplinary reporting and decision making, and we work with university clinics, hospitals, radiological practices, CROs, pharmaceutical and biotech companies worldwide.
Job Description
We are looking for a Project Engineer to support the setup, verification, documentation, and improvement of clinical trial configurations in our software platform. You will work closely with customer-facing and R&D teams to translate study requirements into high-quality system configurations and documentation. Your work will directly impact the success of international imaging research projects by ensuring trials are configured accurately and efficiently.
Key Responsibilities
- Configure and maintain clinical trials within the mint Lesion™ software platform for international research and clinical trial central reads.
- Translate clinical study requirements into structured, high-quality system configurations.
- Design and assemble tailored configuration packages for customer-specific trial instances.
- Manage and update configurations on customer environments throughout the study lifecycle.
- Create and refine standardized Configuration Specification Templates (MCS) to ensure scalability and consistency.
- Verify and validate trial configurations for accuracy, completeness, and compliance with specifications.
- Document configurations in a structured and traceable manner according to internal processes.
- Act as a bridge between customer success and R&D teams to improve configuration capabilities and processes.
Qualifications
- Technical or scientific academic degree (e.g., Life Sciences, Medical Imaging, Healthcare, Engineering, IT) or equivalent work experience.
- Experience in imaging clinical trials (preferably oncology), CRO processes, or clinical operations is strongly preferred.
- Knowledge of, or certification in, ICH GCP and/or FDA CFR 21 part 11 is strongly preferred.
- Strong technical understanding and comfort working with complex configurable software systems and structured data.
- Excellent analytical skills and a structured, quality-driven approach.
- Strong communication skills in English; ability to work with international teams across time zones.
Additional Information
- Supportive international team and culture of trust.
- Meaningful responsibilities impacting global healthtech and patient outcomes.
- 30 vacation days, plus December 24th and 31st.
- Flexible working hours and a hybrid work model within Germany.
- Bike leasing via partner “BikeLeasing” and Urban Sports Club membership with employer contribution.
- Regular after‑work, team, and company events.
How to Apply
Please apply online via the "Apply Now" button on the job page. Submit your CV, your first available start date, and your desired salary.
Contact
HR Contact Person: Tatjana von Freyberg, Manager Recruiting. For general inquiries you may use [email protected].