At Merck, we ensure high quality clinical trials by integrating state-of-the-art technology and applying rigorous scientific and ethical standards. We are seeking a Clinical Database Testing Analyst I to join the Global Clinical Data Integration department. In this temporary position, you will execute validation activities to uphold data quality and system integrity for clinical trials.
What You'll Do
- Execute and document validation activities for standard and study-specific test cases, including recording test data and results and preparing validation summary reports.
- Coordinate and conduct User Acceptance Testing (UAT).
- Create trial-specific test cases.
- Develop data integrity and consistency checks across data pipelines, integrations, and automation workflows.
- File essential records in the official repository, maintain traceable evidence, and ensure audit-ready documentation.
- Develop, review and maintain UAT release documents for trial-based configuration, including any change control documents.
What We're Looking For
- B.A. or B.S. degree or student, preferably in mathematics, science, health care related disciplines, or computer science.
- English proficiency at the C1 level.
- Familiarity with clinical data management systems and platforms.
- Familiarity with a test management solution such as Jira Xray.
- Understanding of GxP, computer system validation (CSV), and other regulatory guidelines.
- Basic knowledge of system development lifecycle management.
- Ability to follow good documentation and testing practices.
- Coordination skills to oversee timelines, resources and team deliverables.
- Ability to communicate clearly with both technical and non-technical stakeholders and to facilitate communication among team members.
- Ability to prioritize work effectively and meet deadlines, maintaining high standards of accuracy and data integrity.
- Ability to work both independently and collaboratively within diverse teams.
- Demonstrated accountability, adaptability, and analytical problem-solving.
- Skills and knowledge areas including: Automation in Systems Integration, Clinical Data Cleaning, Clinical Data Management, Clinical Documentation, Clinical Trials, Communication, Computer Science, Cross-Cultural Teams, Data Analysis, Data Documentation, Data Entry, Data Integrity, Data Processing, Data Quality, Data Quality Control, Data Reporting, Data Review, Data Validation, Data Visualization, and Good Clinical Practice (GCP).
Technical Stack
- Clinical data management systems and platforms
- Test management solution (e.g., Jira Xray)
Team & Environment
You will be part of the Global Clinical Data Integration (GCDI) department.
Work Mode
This position follows a hybrid work model.
Merck is an equal opportunity employer.
