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Senior Rave Clinical Database Programmer

Katalyst Healthcares and Lifesciences

Remote or New York, New York • Today

Full-time

Senior Database Engineer

London Stock Exchange Group

New York, New York • Today

Full-time

USD 100,200.00 - 167,000.00 per year

Senior Database Engineer

London Stock Exchange Group

New York, New York • 23d ago

Full-time

USD 100,200.00 - 167,000.00 per year

Senior Clinical Data Analyst

Tranzeal, Inc.

Remote • Today

Easy Apply

Contract

$55 - $60

Urgent Need - Data Quality Lead with Clinical Data Exp - 100% Remote

Komplete Teleservices

Remote • Today

Easy Apply

Contract

Depends on Experience

Senior Database Administrator

Leviton Manufacturing

Remote or Melville, New York • Today

Full-time

USD 140,000.00 per year

Senior Database Developer

Dizer Corp

Hybrid in New York, New York • 15d ago

Easy Apply

Contract

45 - 50

Senior Database Engineer

Jean Martin, Inc

Hybrid in Fort Lee, New Jersey • 10d ago

Easy Apply

Full-time, Third Party

Depends on Experience

Senior Database Administrator

Jean Martin, Inc

Fort Lee, New Jersey • 7d ago

Easy Apply

Contract, Third Party

Depends on Experience

Senior Cyber Database Engineer - Data Protection/DLP

Quality Business Engineering

Remote or Haymarket, Virginia • Today

Full-time

USD 105,000.00 - 120,000.00 per year

Clinical Data Integration Lead

Spadtek Solutions LLC

New Milford, New Jersey • Yesterday

Easy Apply

Contract, Third Party

Depends on Experience

Senior Database Performance Engineer

AmeriSave Mortgage Corporation

Remote or Enterprise, Oregon • Today

Full-time

USD 100,000.00 - 170,000.00 per year

Senior Lead Database Reliability Engineer

DraftKings

Remote • Today

Full-time

USD 168,000.00 per year

Senior Database Reliability Engineer

Scribe

Remote or San Francisco, California • Today

Full-time

USD 145,000.00 - 230,000.00 per year

Senior Mainframe DB2 & IMS System Programmer

Tixy Services LLC

Remote • 10d ago

Easy Apply

Contract

Depends on Experience

Senior Clinical Data Analyst – SQL & BigQuery

Datamatics Global Services, Inc.

Remote • Today

Easy Apply

Full-time

Depends on Experience

Senior Engineer, Database and OS Developer

Intraedge

Remote • 27d ago

Easy Apply

Contract, Third Party

Depends on Experience

Senior Database Administrator

VISION INFOTECH INC.

Remote • Yesterday

Easy Apply

Contract, Third Party

Depends on Experience

SQL Server Database Senior Developer, Vice President

MUFG

New York, New York • Today

Full-time

USD 147,000.00 - 205,000.00 per year

Database Administrator - Senior

ASM Research

Remote • Today

Full-time

Senior Clinical Database Programmer

Katalyst Healthcares and Lifesciences

Edison, New Jersey • Today

Full-time

Senior Database Developer

Cantor Fitzgerald Securities

New York, New York • 14d ago

Full-time

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 6 hours ago

Fitment

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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

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.

Dice Id: 91116760
Position Id: dab2c2aa6a1210f032cf5565271212dd
Posted 6 hours ago

Fitment

Dice Job Match Score™

🔢 Crunching numbers...

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