Join Cyntegrity, one of the leading clinical trial risk management technology providers in the industry. We're proud of our highly rated MyRBQM® Portal and MyRBQM® Academy brands.
If you’re passionate about data, technology, and innovation in healthcare — and you’re looking to join a fast-growing, purpose-driven company — this is an exciting opportunity for you.
Our international and collaborative team is looking for a Quality Assurance (QA) Data Engineer to support the development and optimization of our data pipelines, datasets, and KRI (Key Risk Indicator) systems that power clinical trial insights and analytics. You will own the data quality lifecycle—from ingestion and mapping through validation, lineage, and audit—working closely with R&D, Data Science, and QA.
Key Responsibilities
- Develop, maintain, and optimize structured and unstructured datasets with strong traceability and audit readiness.
- Design and implement data mappings from raw clinical data to Cyntegrity’s internal formats.
- Enhance data quality, consistency, and efficiency across systems by implementing automated data quality checks and monitoring.
- Collaborate with R&D, Data Science, and QA teams to ensure alignment with business and regulatory requirements.
- Support data transformation, ETL, and integration processes.
- Work with both legacy and new code to improve scalability and reliability of data systems.
- Contribute to risk management and compliance efforts across regulated environments.
- Prepare realistic test datasets (synthetic and de-identified) to validate metrics across potential clinical scenarios; design scenario-based validation test dataset and acceptance criteria.
Essential Criteria
Education
- Bachelor’s or Master’s degree in Computer Science, Software Engineering, or a related field.
Experience / Skills
- 3+ years of software programming experience (Data engineering or back-end focus preferred).
- 2+ years of experience with .NET, Python, or other scripting languages.
- Hands-on SQL expertise (query performance, modeling, and data profiling).
- Experience with agile product development lifecycle.
- Proficiency in data transformation, ETL, and pipeline development.
- Proven implementation of automated data quality checks, validation rules, and monitoring (e.g., unit/integration tests for data, expectations-based testing).
- Familiarity with clinical data standards (e.g., CDISC SDTM/ADaM) and common source formats from EDC, labs, and safety systems is a plus.
- Experience generating synthetic or de-identified datasets.
- Familiarity with risk management concepts and process-oriented environments.
- Comfortable working remotely and delivering measurable results.
- Strong troubleshooting, communication, and problem-solving skills.
- Willingness to work with both legacy systems and new architectures.
- Working knowledge of written and spoken English.
Knowledge (Technical Proficiency)
- Programming Languages: Python, R, JavaScript, .NET C#
- Data Formats: XML/XPATH, JSON, SAS, CSV, Excel
- Databases: MongoDB, SQL (familiarity with data warehouses/lakehouses is a plus).
- Technologies: Docker, Linux, Bash, Azure DevOps (or similar tools), ETL pipelines
- Bonus: Azure cloud experience or certifications
- Plus: Domain knowledge in clinical trials, data standards, and applied statistics
- Familiarity with CFR 21 Part 11, ICH GCP, and FDA Software Validation Guidance; Understanding of GDPR and data privacy best practices
Compensation
- Full-time employment
- Competitive salary
- Remote work flexibility
About Cyntegrity
We support sponsors and CROs with clinical trial risk management technology and educational programs to bring therapies to market faster, safer, and more efficiently.
Cyntegrity is a fast-growing, international company driven by innovation and quality. We aim to be the first-choice provider of specialized cloud and SaaS solutions for ICH GCP E6(R3)-compliant risk-based quality management and clinical research.
Learn more about us and our brands at www.cyntegrity.com
If this is a position of your interest, and you would like to know more or have any additional questions, please submit your application.
