Clario Holdings Inc.
Software Development Engineer II (f/m/d)
Clario Holdings Inc., New Bremen, Ohio, United States
Software Development Engineer II (f/m/d) page is loaded## Software Development Engineer II (f/m/d)locations:
Estenfeld, Germanytime type:
Full timeposted on:
Posted Todayjob requisition id:
R16802We are looking for you as **Software Development Engineer II (f/m/d)** at our Clario site in Estenfeld (near Würzburg) for developing and successfully delivering a project-specific highly-interactive mobile-web and other software applications for clinical research data acquisition and data management that is deployed onto worldwide distributed Smartphones, Tablets and Asthma monitor devices.Become a part of driving clinical studies forward faster with your daily performance with us. You will be responsible for ensuring that our customers (pharmaceutical companies, BioTechs, and CROs)receive software applications according to the study specifications*.*Even if you don't have experience in the world of clinical trials, we'd love to show you!**What we offer*** Flexible working hours and working time accounts to support the work-life balance* Working from home 50% of your time, since you can do a big amount of your required work either hybrid or remote* Support your professional development through internal and external training and certification programs* Salary plus Annual bonus target* Company pension scheme**What you'll be doing**Join our team of international Software Development Engineers! We're excited to welcome a new team member who can support projects and collaborate on technical questions.* Work collaboratively within an international team of Software Development Engineers, supporting projects and addressing technical questions.* Develop, deploy, and maintain software applications based on clinical trial software specifications.* Integrate acquired device data with backend project-specific databases.* Participate in decision-making throughout the development life cycle of clinical trial study data collection applications.* Contribute to project specification development and the planning and deployment scheduling process.* Review moderate to high-complexity code from other engineers and write your own high-quality code.* Communicate timelines, scope, and technical concerns effectively to internal stakeholders.* Present technical decisions through presentations, tech talks, and wiki documentation.* Collaborate with cross-functional teams, including Design, Quality, Translations, and Project Management, to ensure project success.* Negotiate and resolve study team issues related to timelines, schedules, and technical changes.**What we look for*** Degree in Computer Science or a related field (or equivalent experience).* 3+ years of software development experience.* Proficiency in English (spoken and written).* Availability to work on-site as needed due to hardware dependencies.* Strong ability to prioritize multiple projects in a fast-paced environment with tight timelines.* Technical expertise in C/C++, .NET/C#, Angular, and JavaScript.At Clario, our purpose is to transform lives by unlocking better evidence. It’s a cause that unites and inspires us. It’s why we come to work—and how we empower our people to make a positive impact every day. Whether you're advancing clinical science, building innovative technology, or supporting our global teams, your work helps bring life-changing therapies to patients faster.Clario is a leading provider of endpoint data solutions to the clinical trials industry, generating high-quality clinical evidence for life sciences companies. We offer comprehensive evidence generation solutions that combine medical imaging, eCOA, precision motion, cardiac solutions and respiratory endpoints.For more than 50 years, Clario has delivered deep scientific expertise and broad endpoint technologies to help transform lives around the world. Our endpoint data solutions have supported over 30,000 clinical trials in more than 100 countries. Our global team of science, technology, and operational experts have supported over 70% of all FDA drug approvals since 2015. #J-18808-Ljbffr
Estenfeld, Germanytime type:
Full timeposted on:
Posted Todayjob requisition id:
R16802We are looking for you as **Software Development Engineer II (f/m/d)** at our Clario site in Estenfeld (near Würzburg) for developing and successfully delivering a project-specific highly-interactive mobile-web and other software applications for clinical research data acquisition and data management that is deployed onto worldwide distributed Smartphones, Tablets and Asthma monitor devices.Become a part of driving clinical studies forward faster with your daily performance with us. You will be responsible for ensuring that our customers (pharmaceutical companies, BioTechs, and CROs)receive software applications according to the study specifications*.*Even if you don't have experience in the world of clinical trials, we'd love to show you!**What we offer*** Flexible working hours and working time accounts to support the work-life balance* Working from home 50% of your time, since you can do a big amount of your required work either hybrid or remote* Support your professional development through internal and external training and certification programs* Salary plus Annual bonus target* Company pension scheme**What you'll be doing**Join our team of international Software Development Engineers! We're excited to welcome a new team member who can support projects and collaborate on technical questions.* Work collaboratively within an international team of Software Development Engineers, supporting projects and addressing technical questions.* Develop, deploy, and maintain software applications based on clinical trial software specifications.* Integrate acquired device data with backend project-specific databases.* Participate in decision-making throughout the development life cycle of clinical trial study data collection applications.* Contribute to project specification development and the planning and deployment scheduling process.* Review moderate to high-complexity code from other engineers and write your own high-quality code.* Communicate timelines, scope, and technical concerns effectively to internal stakeholders.* Present technical decisions through presentations, tech talks, and wiki documentation.* Collaborate with cross-functional teams, including Design, Quality, Translations, and Project Management, to ensure project success.* Negotiate and resolve study team issues related to timelines, schedules, and technical changes.**What we look for*** Degree in Computer Science or a related field (or equivalent experience).* 3+ years of software development experience.* Proficiency in English (spoken and written).* Availability to work on-site as needed due to hardware dependencies.* Strong ability to prioritize multiple projects in a fast-paced environment with tight timelines.* Technical expertise in C/C++, .NET/C#, Angular, and JavaScript.At Clario, our purpose is to transform lives by unlocking better evidence. It’s a cause that unites and inspires us. It’s why we come to work—and how we empower our people to make a positive impact every day. Whether you're advancing clinical science, building innovative technology, or supporting our global teams, your work helps bring life-changing therapies to patients faster.Clario is a leading provider of endpoint data solutions to the clinical trials industry, generating high-quality clinical evidence for life sciences companies. We offer comprehensive evidence generation solutions that combine medical imaging, eCOA, precision motion, cardiac solutions and respiratory endpoints.For more than 50 years, Clario has delivered deep scientific expertise and broad endpoint technologies to help transform lives around the world. Our endpoint data solutions have supported over 30,000 clinical trials in more than 100 countries. Our global team of science, technology, and operational experts have supported over 70% of all FDA drug approvals since 2015. #J-18808-Ljbffr