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# Clinical database EDC programmer

- **Company:** Mindlance
- **Location:** United States (Remote available)
- **Experience:** Experienced
- **Salary:** $104,000.0 - $114,400.0
- **Contract:** Temporary contract
- **Skills:** Databases, Data Streaming, Information Technology
- **Published:** August 24, 2026
- **Apply:** https://www.indeed.com/viewjob?jk=67ac72b7f49bd27f

## About the Role

Core Requirements

 * Medidata Rave Certification with 3+ years of hands-on study build experience
 * Strong communication and presentation skills
 * Ability to work in a fast-changing, evolving environment

Technical & Clinical Expertise

 * 3+ years of clinical technology (EDC) experience or
 * 5+ years in a similar technical or clinical development role
 * Demonstrated understanding of the clinical trial process
 * Knowledge of CDASH and SDTM
 * Experience with common industry design and development tools
 * Experience with EDC integrations (e.g., IRT)Professional Skills
 * Strong analytical and problem-solving skills
 * Ability to manage multiple priorities and timelines
 * Proven ability to influence stakeholders without direct authority

Education

 * Bachelor's degree in Business, MIS, Computer Science, Life Sciences, or equivalent experience
 * Master's degree preferred, 1. Are you Medidata Rave Certified Study Builder?
 2. How many years of experience do you have with EDC study builds?

## Description

EDC Design & Delivery

 * Translate study protocol requirements into Electronic Data Capture (EDC) system design
 * Ensure use of common data standards across studies
 * Design EDC systems to optimize functionality, end-user experience, and data flow
 * Own on-time delivery of EDC builds, amendments, and system changes
 * Manage integrations between EDC and other systems (e.g., IRT)

Study & Program Execution

 * Ensure TA- and program-level consistency across studies
 * Track study progress using project management tools
 * Anticipate risks to timelines or quality and develop mitigation plans
 * Ensure work products align with upstream and downstream dependencies

Cross-Functional Collaboration

 * Partner with DSS and cross-functional stakeholders to meet study and program objectives
 * Influence team members without direct authority
 * Participate in innovation and process-improvement initiatives

Compliance & Quality

 * Ensure adherence to federal and local regulations
 * Ensure compliance with GCP, ICH guidelines, SOPs, and quality standards
 * Stay current on evolving regulations and clinical development policies


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