Join AutoProff – Help Shape the Future of Automotive Tech! 🚀🏎️ 

We are looking for a new colleague to join our talented Technology team based at our Vejle office. 

At AutoProff, we believe great technology drives great experiences—and we’re just getting started. We’re on a mission to transform the way vehicles are traded across Europe, and we need curious and driven new colleagues to help us do it. 

As our new Senior Software Engineer, you’ll join a cross-functional team responsible for building a unified seller solution that powers how vehicles enter and move through the AutoProff platform. We focus on enabling dealers to efficiently manage, price, and sell their inventory by combining streamlined vehicle intake, data-driven pricing, and intuitive seller tools. Our work simplifies trade-ins, improves sourcing decisions, and helps dealers act faster and more confidently, ultimately unlocking value earlier in the vehicle lifecycle. 

We foster a developer-friendly culture where innovation isn’t just encouraged; it’s expected. You’ll have access to modern, AI-powered tools to enhance productivity and streamline your daily work. We host hackathons to explore new tech, ideas and tools, and our internal developer forums are open spaces for discussing architecture, new technologies, and tough engineering challenges. Whether building or learning, there's always room to experiment and grow. 

Let's dive into your key responsibilities. You will: 

• Work in a dynamic and international environment with experienced and skilled colleagues 

• Design, develop, and maintain efficient, reusable, and reliable code using engineering best practices and design patterns. 

• Drive a culture of “you build it - you own it” - mentality 

• Identify and act on areas for your own personal development 

• Mentor and coach co-workers on topics that you master. 

The need-to-have skills 

• Proven ability to thrive in environments that value adaptability, shared ownership, and continuous improvement 

• Experience working with .NET and C# 

• Strong understanding of object-oriented programming, distributed systems and event-driven architecture. 

• Experience with relational databases or No-SQL databases 

• Good communication skills and fluency in business English (spoken and written) 

• Open towards and able to quickly learn new technologies 

• Ability to troubleshoot problems, debug and suggest solutions 

• A pragmatic and responsible approach to GenAI, understanding its limitations and risks, and actively establishing guardrails (e.g. reviews, testing, and policies) to ensure safe, compliant, and scalable use in production environments. 

The nice-to-have skills 

• Experience working with AWS Infrastructure or other cloud providers, especially containerization and serverless computing. 

• Experience with RESTful APIs 

We’re eager to hear from you! If this sounds like a great match and sparks your interest, don’t wait, apply today! 

About AutoProff 

AutoProff was founded in 2013 by the experienced car dealer Jesper Ratza in Denmark. The aim was to digitalize B2B used car trading, helping car dealers increase sales and improve profits.  

in August 2022, AutoScout24, the leading specialized pan-European online car marketplace, acquired a majority stake in AutoProff. The partnership has supported the rapid expansion of AutoProff's solutions across Europe and enables the creation of Europe's first fully integrated C2B-B2B-B2C dealing solution for used cars.  

At AutoProff, we specialize in providing online B2B used-car dealing solutions designed to improve the buying and selling experience for professional car dealers and their customers. 

We are the emerging European leader with more than 150,000 B2B used cars on our online trading platforms annually.    

With a focus on effective solutions, digitization and customer service, we are committed to being the home of B2B car dealing for European car dealers.  

Your role:

• Schedule, Plan and Conduct Site Visits: Site Selection Visits, Site Initiation Visits, Interim Monitoring Visits and Site Close-out Visits.
• Write Reports and Investigator Follow-up Letters for Site Visits: Site Selection Visits, Site Initiation Visits, Interim Monitoring Visits and Site Close-out Visits.
• Manages the progress of assigned studies by tracking regulatory/ IRB submissions and approvals, recruitment and enrolment, CRF completion and submission, and data query generation and resolution
• Provide project updates to project management team.
• Organize delivery of investigational product, laboratory supplies, CRFs and other study specific materials to and from the clinical sites.
• Perform investigational product inventory and ensure return of unused investigational product to designated location or verify destruction as required.
• Assists with, prepare for, and attends Investigator Meetings for assigned studies.
• Review study documents for compliance with protocol, ICH GCP guidelines, Protocol Deviations/Violations and Waivers, review study documents for subject safety events; escalate issues at site to project management.
• Collect and review essential study documents from site for filing in eTMF.
• Administers protocol and related study training to assigned sites and establishes regular lines of communication with sites to manage ongoing project expectations and issues.
• Evaluates quality and integrity of study site practices related to the proper conduct of the study and ensure adherence to applicable regulations.
• Compliances: Follow international GCP guidelines/regulations and SOPs for executing clinical studies. Participates in the planning of quality assurance activities and coordinates resolution of audit findings.
• Assists the Clinical Trial Manager with clinical operations activities by overseeing resource allocation, reviewing site performance, providing feedback to CRAs and CTAs, resolving issues, performing review and oversight of site visit reports.
• May review protocols, eCRFs, study manuals and other study related documents, as requested by the Clinical Trial Manager.
• May conduct on-site evaluation visits and on-site training of CRAs
• Lead and partake in regular team meeting / teleconferences.
• Assist, as appropriate, with reporting site performance regarding timelines and deliverables during project team meetings and assist with providing and compiling feedback for analysis of overall study performance.
• May serve as mentor to associates on the subject of job performance, trainings and professional growth.
• Other duties as assigned. 

Your Profile:

• Bachelor’s Degree in biomedical sciences or related scientific discipline
• Fluent English (oral and written) and applicable local business language.
• Minimum three years of monitoring experience, more experience preferred, with a combination of clinical research coordinator and or other relevant clinical research experience.
• Sound knowledge of medical terminology and advanced proficiency in clinical monitoring process.
• Ability to travel up to 70%, depending on project requirements.
• Good knowledge and understanding of ICH GCP and worldwide applicable regulatory requirements
• Good leadership, planning, project management skills, verbal communication skills, and written communication skills.
• Knowledge and experience with MS Office suite (at a minimum Word, PowerPoint and Excel).

If you have the experience required and want to join an energetic, creative, and collaborative team, please apply directly to our website at https://biorasi.com or email us at careers@biorasi.com.