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Senior Rave Clinical Database Programmer

Katalyst Healthcares and Lifesciences

Remote or New York, New York • 3d ago

Full-time

Senior RAVE Clinical Database Programmer

Katalyst Healthcares and Lifesciences

Remote or New Jersey • 3d ago

Full-time

Clinical Database Programmer

Becton Dickinson & Company

Remote or Maryland • Today

Full-time

Senior Database Developer

RSM US LLP

New York, New York • Today

Full-time

Sr Clinical Data Management Associate

Gilead Sciences, Inc.

Remote • Today

Full-time

USD 115,260.00 - 149,160.00 per year

Senior Database Developer - C13

Citi

Jersey City, New Jersey • Today

Full-time

USD 142,320.00 - 213,480.00 per year

Senior Database Engineer

London Stock Exchange Group

New York, New York • Today

Full-time

USD 100,200.00 - 167,000.00 per year

Senior RPA Developer

Raas Infotek LLC

Hybrid in New York, New York • 2d ago

Easy Apply

Contract

55 - 60

Senior Associate, Clinical Data Standards Management (CDSM)

Gilead Sciences, Inc.

Remote • Today

Full-time

USD 123,930.00 - 160,380.00 per year

Senior Database Platform Engineer

Dimensional Fund Advisors, L.P.

New York, New York • Today

Full-time

Senior Java Big Data Developer - AVP

Citi

Jersey City, New Jersey • Today

Full-time

USD 121,200.00 - 181,800.00 per year

Senior Database Administrator

Leviton Manufacturing

Remote or Melville, New York • Today

Full-time

USD 140,000.00 per year

Senior Database Reliability Engineer

Pro Integrate

Remote or New York, New York • Today

Easy Apply

Full-time

$$220K - $260K/yr compensation

Senior Database Administrator

General Dynamics

Remote • Today

Full-time

USD 97,968.00 - 129,950.00 per year

Database Lead

Hallmark Global Technologies

Remote • 3d ago

Easy Apply

Contract

Depends on Experience

Senior Database Engineer

Zelis

Remote • Today

Full-time

USD 105,000.00 - 133,000.00 per year

Senior Database Engineer

Datavail

Remote or Boulder, Colorado • Today

Full-time

Senior Database Administrator – Azure SQL / Amazon RDS / Percona MySQL (Healthcare SaaS)

NDA PARTNERS INC

Remote • 2d ago

Easy Apply

Full-time, Third Party

Depends on Experience

Senior Database Platform Engineer

Dimensional Fund Advisors LP

Remote • Today

Full-time

Senior Database Administrator

ACI Group, Inc.

Remote • 12d ago

Easy Apply

Contract

Depends on Experience

Senior Database Administrator

Greenberg Traurig, LLP

Remote or Chicago, Illinois • Today

Full-time

USD 123,371.00 - 136,060.00 per year

SQL Server Database Senior Developer, Vice President

MUFG

New York, New York • Today

Full-time

USD 147,000.00 - 205,000.00 per year

Senior Clinical Database Programmer

Katalyst Healthcares and Lifesciences

Edison, New Jersey • 3d 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
Problem Solving
Conflict Resolution
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
Problem Solving
Conflict Resolution
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 30+ days ago

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New York, New York

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Today

About Formation Bio Formation Bio is a tech and AI driven pharma company differentiated by radically more efficient drug development. Advancements in AI and drug discovery are creating more candidate drugs than the industry can progress because of the high cost and time of clinical trials. Recognizing that this development bottleneck may ultimately limit the number of new medicines that can reach patients, Formation Bio, founded in 2016 as TrialSpark Inc., has built technology platforms, proces

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Senior Data Scientist - Clinical Informatics (Analytics Enablement)

Remote or New York, New York

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Today

We're building a world of health around every individual - shaping a more connected, convenient and compassionate health experience. At CVS Health , you'll be surrounded by passionate colleagues who care deeply, innovate with purpose, hold ourselves accountable and prioritize safety and quality in everything we do. Join us and be part of something bigger - helping to simplify health care one person, one family and one community at a time. Position Summary CVS Health's Analytics & Behavior Chan

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Senior RAVE Clinical Database Programmer

Remote or New Jersey

•

3d ago

Job Description: 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:

Full-time

Senior Manager, Clinical Programming

Princeton, New Jersey

•

Today

At Genmab, we are dedicated to building extra[not]ordinary futures, together, by developing antibody products and groundbreaking, knock-your-socks-off KYSO antibody medicines that change lives and the future of cancer treatment and serious diseases. We strive to create, champion and maintain a global workplace where individuals' unique contributions are valued and drive innovative solutions to meet the needs of our patients, care partners, families and employees. Our people are compassionate,

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USD 131,040.00 - 196,560.00 per year