Do you want to join us in helping to fight the world’s most threatening diseases and enabling access to care for more people around the world? At Siemens Healthineers, we pioneer breakthroughs in healthcare. For everyone. Everywhere.

We offer you a flexible and dynamic environment with opportunities to go beyond your comfort zone in order to grow personally and professionally. Sound interesting? Then come and join our global team as Senior Staff Database Developer.

Our global team: We are a team of 66,000 highly dedicated employees across more than 70 countries passionately pushing the boundaries of what’s possible in healthcare to help improve people’s lives around the world. As a leader in the industry, we aspire to create better outcomes and experiences for patients no matter where they live or what health issues they are facing. Our portfolio, spanning from in-vitro and in-vivo diagnostics to image-guided therapy and innovative cancer care, is crucial for clinical decision-making and treatment pathways.

Our culture: We are part of an incredible community of scientists, clinicians, developers, researchers, professionals, and skilled specialists pushing the boundaries of what’s possible, to improve people’s lives around the world. We embrace a culture of inclusivity in which the power and potential of every individual can be unleashed. We spark ideas that lead to positive impact and continued success. Check our Careers Site at https://www.siemens-healthineers.com/en-us/careers.

The Senior Staff Database Developer provides technical direction for the design, development, implementation, and verification of electronic data capture (EDC) requirements and electronic case report forms (eCRFs) within clinical data management systems at Siemens Healthineers.The role involves interfacing with clinical data managers, statisticians, clinical affairs representatives, and external partners and vendors to design, configure, test, implement, maintain, and execute changes to the clinical database systems. They will also be involved in troubleshooting any issues on behalf of users and maintaining data standards across various therapeutic areas.They will act as technical expert for the clinical data management system. The senior staff database developer will provide technical guidance, direction, and training to data management, clinical affairs, and statistical affairs staff on data management practices and database systems. They will provide technical oversight to the activities of junior clinical data management staff or contractors. They will serve as a prime point of technical contact and interface for database vendors.

The Senior Staff database Developer will be responsible for maintaining knowledge of state-of-the-art clinical data management practices. The role will be expected to pro-actively identify issues and opportunities with current clinical data management processes and systems. They will provide input to senior management on process improvement and long-term strategies for clinical data management.

The position will report to the Director of Data Management within Biostatistics, Analytics, & Data Management.

Duties & Responsibilities:

• In conjunction with clinical study team, develops, implements, and tests requirements (key variables, CRFs, edit checks, etc.) for electronic data capture of clinical trial data
• Provides guidance and training to clinical affairs, statistical affairs, data management, and R&D Staff on EDC tools
• Maintains data standards and medical dictionaries within the clinical EDC system
• Maintains compliance to regulations (HIPAA, Data Protection Act, etc.)
• Develops reports to support study monitoring, data cleaning and verifications of data quality
• Manages user access and permissions within the clinical EDC system (e, g., OpenClinica, Medrio, Medidata Rave)
• Monitors performance of the Clinical EDC and manages parameters to provide fast responses to front-end users
• Translates protocol requirements into requirements for EDC and/or eCRFs
• Makes design decisions with input from end-users at trial sites, study monitors, biostatisticians, etc.

Required Knowledge/Skills, Education, and Experience

• Master’s degree in Bioinformatics, Computational Biology, Computer Science (Relational Database Systems emphasis), or Software Engineering
• 9+ years within clinical data management or software engineering support of EDC systems and applications
• Experience working within a Clinical EDC system (e.g., OpenClinica, Medrio, Medidata Rave)

• Experience with Laboratory Information Management Systems (LIS/LIMS)
• Knowledge of SAS, R, Python programming
• Proficiency with the following programming languages: C#, ASP.NET, HTML
• Working knowledge within areas of Good Clinical Practices, Good Clinical Data Management Practices, Design and Conduct of Clinical Trials/Studies, and related regulatory requirements and terminology
• Experience within Microsoft Office Suites (Word, Excel, PowerPoint)
• Exposure to clinical data coding classification systems, e.g., MedDRA, WHO-Drug, Data Standardization (CDISC STDM &/or ADAM), Meta-Data Repository
• Strong interpersonal, organizational, and communication skills
• Excellent attention to detail and problem-solving skills
• Ability to work effectively in a team setting

The pay range for this position is $131,920 - $181,390.00 annually; however, base pay offered may vary depending on job-related knowledge, skills, and experience. The annual incentive target is (15%) of base pay. Siemens Healthineers offers a variety of health and wellness benefits including paid time off and holiday pay. Details regarding our benefits can be found here: https://benefitsatshs.com/index.html

This information is provided per the required state Equal Pay Act. Base pay information is based on market location. Applicants should apply via Siemens Healthineers external or internal careers site.

At Siemens Healthineers, we value those who dedicate their energy and passion to a greater cause. Our people make us unique as an employer in the med-tech industry. What unites and motivates our global team is the inspiration of our common purpose: To innovate for healthcare, building on our remarkable legacy of pioneering ideas that translate into even better healthcare products and services. We recognize that taking ownership of our work allows both us and the company to grow. We offer you a flexible and dynamic environment and the space to move beyond your comfort zone to grow both personally and professionally.

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If you want to join us in transforming the way healthcare is delivered, visit our career site at https://usa.healthcare.siemens.com/careers.

If you wish to find out more about the specific before applying, please visit: https://usa.healthcare.siemens.com/about.

“Successful candidate must be able to work with controlled technology in accordance with US export control law.” “It is Siemens Healthineers’ policy to comply fully and completely with all United States export control laws and regulations, including those implemented by the Department of Commerce through the Export Administration Regulations (EAR), by the Department of State through the International Traffic in Arms Regulations (ITAR), and by the Treasury Department through the Office of Foreign Assets Control (OFAC) sanctions regulations.”

As an equal-opportunity employer we are happy to consider applications from individuals with disabilities.