Clinical Programmer

## Clinical Programmer Apply:
Hybrid:
CRI
- San Jose
- San Jose (City Place):
Full time:
Posted Today:
End Date:
October 20, 2026 (7 days left to apply):
R421858

Job Description
* Activities may include, but are not limited to:
* · Build, integrate, and maintain clinical databases and study systems, including transformations, edit checks, reporting, and user testing, while supporting governance of cross‐study programming environments.
· Design, develop, test, and maintain clinical technology systems (EDC, RTSM, eCOA/ePRO) using programming and automation frameworks.
· Implement and validate complex data logic such as edit checks, derivations, and dynamic rules.
· Propose and develop tools to streamline design, build, and validation workflows.
· Apply data literacy to convert collected data into actionable insights.
· Develop advanced reporting solutions, including dashboards and visual analytics, using enterprise platforms.
· Configure, test, and validate data sources for integrations and transformations across systems.
· Collaborate with stakeholders to translate business needs into technical and system requirements.
· Troubleshoot routine data ingestion and consumption issues, escalating non‐standard problems appropriately.
· Develop robust data models, semantic layers, and curated datasets while monitoring pipelines and enforcing quality checks.
· Validate system functionality and ensure adherence to SOPs, regulations, and compliance standards.
· Identify process gaps and contribute to continuous improvement initiatives.
· Maintain audit‐ready documentation for changes, incidents, and system updates.
· Mentor junior colleagues and contribute to onboarding and knowledge sharing.
· Support release management activities, including change control and risk assessment.
· Lead UAT activities, translate requirements into technical specifications, and refine reporting standards.
· Communicate data and technical findings clearly and partner across teams to enable coordinated, high‐quality delivery.
** Education*
* · B.A. or B.S. degree, preferably in Biotechnology (primary focus). Candidates from Computer Science, healthcare‐related disciplines, or those with relevant skills and experience may also be considered.  
** Experience*
* · Minimum of 3 years experience working in in clinical data programming, data engineering, or related data-management/clinical operations functions.  
** Technical Skills*
* · Proficiency in multiple programming languages (SQL, Python, SAS, R) for implementing data collectors, integrations, transformations, and reporting.
· Skilled with key data‐management tools and platforms, with the ability to adopt new technologies with guidance.
· Able to execute technical tasks independently on straightforward work, seeking moderate guidance for non‐standard activities.
· Experienced in scripting and automating data ingestion, cleaning, and reporting processes.
· Strong understanding of clinical data flow across the study lifecycle (collection, processing, review, reconciliation, reporting).
· Familiarity with clinical and regulatory data standards, clinical operations, and typical clinical trial data structures.
· Knowledge of SDLC and validation practices, including change control, release checklists, and traceability.
· Understanding of GCP, data integrity, audit‐ready documentation, and UAT/sign‐off procedures.
· Experience optimizing reporting performance and applying data quality controls.
· Ability to link business needs to technical deliverables using standard procedures.
· English proficiency of at least B2+ level.  
** Soft Skills*
* · Prioritizes tasks, meets deadlines, and maintains clear, organized documentation.
· Communicates effectively with technical and business partners, adapting style to the…