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Senior Rave Clinical Database Programmer

Remote in New York, NY, US • Posted 4 hours ago • Updated 4 hours ago

Full Time

On-site

Fitment

Dice Job Match Score™

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Job Details

Skills

Reporting
Clinical Trials
Database Design
CDMS
Data Validation
Test Scripts
TMF
Documentation
Impact Analysis
Risk Assessment
Database Migration
Database Administration
Biostatistics
Conflict Resolution
Problem Solving
System Integration
Interactive Voice Response
Clinical Trial Management System
Change Request Management
Regulatory Compliance
Knowledge Sharing
Testing
Startups
EDC
System Administration
Management
Forms
Editing
Database
Software Development
Software Development Methodology
Communication
Collaboration
Migration
Data Flow
Data Analysis
Acceptance Testing
Clinical Data Management

Reporting
Clinical Trials
Database Design
CDMS
Data Validation
Test Scripts
TMF
Documentation
Impact Analysis
Risk Assessment
Database Migration
Database Administration
Biostatistics
Conflict Resolution
Problem Solving
System Integration
Interactive Voice Response
Clinical Trial Management System
Change Request Management
Regulatory Compliance
Knowledge Sharing
Testing
Startups
EDC
System Administration
Management
Forms
Editing
Database
Software Development
Software Development Methodology
Communication
Collaboration
Migration
Data Flow
Data Analysis
Acceptance Testing
Clinical Data Management

Summary

Summary:
The Senior RAVE Clinical Database Programmer participates in the design, development, validation, and maintenance of clinical study databases. This individual applies advanced knowledge of CRF design, database configuration, edit check programming, custom programming, reporting, system integrations, and CDMS functionality while partnering closely with Clinical Data Management and cross-functional study teams to support successful clinical trial execution.
Key Responsibilities:

Serve as the primary owner of study-specific database design within the CDMS (e.g., Medidata Rave; experience preferred), leading clinical database programming activities across multiple studies of complex design.
Review database specification documents created by study teams, including CRF Specifications and Data Validation Specifications (DVS).
Build clinical study database CRF screens based on approved CRF Specifications.
Program edit checks, special actions/functions, custom programs, and derivations in accordance with the DVS.
Plan and coordinate edit check test script development, programming, validation, and User Acceptance Testing (UAT) activities. Ensure issues are resolved in a timely manner and produce validation documentation for study teams and the Trial Master File (TMF).
Complete study database updates in accordance with Change Request documentation and procedures, including performing impact analyses and risk assessments for proposed changes.
Lead and support database migration activities, including live study updates and database maintenance.
Partner with Clinical Data Management, Clinical Operations, Biostatistics, and external vendors to coordinate clinical database programming activities and ensure alignment with study timelines and objectives.
Participate in project meetings, contribute to problem-solving discussions, communicate project risks, and proactively escalate issues that may impact timelines, scope, or quality.
Balance multiple study assignments while effectively managing priorities and communicating resource needs.
Troubleshoot and resolve study build, system integration (e.g., IVRS, CTMS), and change request issues using the appropriate applications.
Develop advanced custom programs and functionality as required by study specifications.
Ensure high-quality deliverables by reviewing study-level, program-level, and multi-study core deliverables for accuracy, completeness, and compliance.
Participate in departmental initiatives, user group meetings, and knowledge-sharing activities to promote best practices and awareness of new system features.
Develop detailed study execution plans, including programming, testing, and UAT milestones, providing clear visibility into study startup progress and key deliverables.
Support the ongoing evolution of internal EDC capabilities by serving as a technical resource to cross-functional study teams and helping establish efficient database programming processes.

Required Qualifications:

6+ years of Medidata Rave programming experience.
Experience with Medidata Rave Core Configuration, including study setup, environment configuration, user roles, security, and system administration.
Experience managing URL Administration by configuring and maintaining study URLs, environment access, and application settings to support development, UAT, and production environments.
Experience creating and maintaining Global Libraries to standardize reusable study components, including forms, fields, code lists, edit checks, and other configuration objects across multiple studies.
Experience programming edit checks, derivations, custom functions, and database updates.
Experience supporting live studies, database amendments, and change requests.
Working knowledge of the Software Development Life Cycle (SDLC).
Strong written and verbal communication skills with the ability to collaborate effectively across cross-functional teams.

Preferred Qualifications:

Extensive experience supporting live study migrations.
Clinical data management domain knowledge.
Experience with data flow and data analytics.
Experience planning and executing formal User Acceptance Testing (UAT).
Experience supporting sponsor-side Clinical Data Management organizations.

Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.

Dice Id: 91116760
Position Id: dab2c2aa6a1210f032cf5565271212dd
Posted 4 hours ago

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