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Associate Clinical Programmer
At a Glance
- Location
- CRI - San Jose - San Jose (City Place)
- Work Regime
- hybrid
- Employment
- Full time
- Experience
- 1+ years
- Posted
- 2026-07-16
Key Requirements
Required Skills
Domain Knowledge
- Clinical
- Engineering
Requirements
Adaptability, Adaptability, Analytical Problem Solving, Audit Documentation, Business Translations, Clinical Database Programming, Clinical Data Cleaning, Clinical Data Management, Clinical Informatics, Computer Science, Dashboard Reporting, Data Analysis, Data Documentation, Data Engineering, Data Entry, Data Ingestion, Data Literacy, Data Processing, Data Quality, Data Reporting, Data Review, Data Validation, Data Visualization, Good Clinical Practice (GCP), Integration Testing {+ 2 more}
Search Firm Representatives Please Read Carefully
Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities.
Where agency agreements are in place, introductions are position specific.
Responsibilities
Build, integrate, and maintain clinical databases and operational systems, including study setup, transformations, integrations, edit checks, reporting, and user testing.
Support the design, development, testing, and maintenance of clinical technology solutions (e.g., EDC, RTSM, eCOA/ePRO) using programming frameworks and automation tools.
Implement and validate data logic such as edit checks, derivations, and dynamic rules.
Contribute to developing and validating tools that streamline design, build, and validation workflows.
Use data literacy skills to transform collected data into meaningful insights.
Help develop and maintain reporting solutions (dashboards, listings, visualizations).