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Senior Rave Clinical Database Programmer

Katalyst Healthcares and Lifesciences

Remote or New York, New York • 8d ago

Full-time

Senior RAVE Clinical Database Programmer

Katalyst Healthcares and Lifesciences

Remote or New Jersey • 8d ago

Full-time

Clinical Database Programmer

Becton Dickinson & Company

Remote or Maryland • Today

Full-time

Senior Manager, Clinical Programming

Genmab

Princeton, New Jersey • Yesterday

Full-time

USD 131,040.00 - 196,560.00 per year

Senior Database Developer

RSM US LLP

New York, New York • Today

Full-time

Clinical Database Specialist (eCRF Design)

McKesson Corporation

Remote or Texas • Today

Full-time

USD 90,600.00 - 151,000.00 per year

Clinical Database Specialist (eCRF Design)

US Venture, Inc.

Remote or Texas • Today

Full-time

USD 90,600.00 - 151,000.00 per year

Senior Database Developer (3292 RBC)

INSPYR Solutions

Remote • 9d ago

Easy Apply

Contract

$50

Sr. Mngr or A.D., Clinical Data Manager

Eliassen Group

Remote or Almont, Colorado • Today

Contract

Principal Clinical Datawarehouse Programmer

BeiGene, Inc.

Remote • Today

Full-time

USD 125,000.00 - 165,000.00 per year

Senior Associate, Clinical Data Standards Management (CDSM)

Gilead Sciences, Inc.

Remote • Today

Full-time

USD 123,930.00 - 160,380.00 per year

Senior Data Analyst, Healthcare Payer Side, Clinical Programs - Full Time, Direct Only

Stone Search

Remote • 16d ago

Easy Apply

Full-time

110,000 - 130,000

Senior Clinical Systems Administrator

Bausch & Lomb

Remote or Oregon • Today

Full-time

USD 85,000.00 - 115,000.00 per year

Senior Database Developer

Kforce Technology Staffing

Remote or Chicago, Illinois • Today

Contract

$50 - $50 hourly

Senior Database Engineer

Zelis

Remote • 2d ago

Full-time

USD 105,000.00 - 133,000.00 per year

Senior Database Engineer

Datavail

Remote or Boulder, Colorado • Today

Full-time

Clinical Data Integration Lead

S Linx LLC

New York, New York • 17d ago

Easy Apply

Contract, Third Party

60 - 65

Technical Support Engineer (New York/New Jersey)

Dassault Systems Americas Corp.

Woodbridge Township, New Jersey • Today

Full-time

USD 79,500.00 - 106,000.00 per year

Senior Clinical Data Analyst (Healthcare Analytics)

Tendo

Remote or Chicago, Illinois • Today

Full-time

USD 97,750.00 - 132,250.00 per year

Placement Role - Senior Technical Architect Algo Design for Clinical Imaging with AWS and AI/ML exp- Remote

Infinity Tech Group Inc

Remote • Yesterday

Easy Apply

Contract

Depends on Experience

Senior Applications Engineer

Dassault Systems Americas Corp.

Woodbridge Township, New Jersey • Today

Full-time

USD 114,750.00 - 153,000.00 per year

Sr Mngr, Full Stack Clinical Platform Engineer

Eliassen Group

Remote or Almont, Colorado • Today

Contract

Senior Software Engineer

Formation Bio

New York, New York • Today

Full-time

USD 185,500.00 - 232,000.00 per year

(PALM) and Artificial Intelligence Co-Op

Johnson & Johnson

Hopewell Township, New Jersey • Today

Full-time

USD 23.50 per hour

Associate Director, Clinical Data Management

Genmab

Princeton, New Jersey • Yesterday

Full-time

USD 157,360.00 - 236,040.00 per year

Senior Director, Information Technology (BioPharma)

Robert Half

Morristown, New Jersey • Today

Easy Apply

Full-time

USD 210,000.00 - 255,000.00 per year

Senior Staff Applications Engineer

Dassault Systems Americas Corp.

New York, New York • Today

Full-time

USD 157,500.00 - 210,000.00 per year

Senior Site Reliability Engineer

Formation Bio

New York, New York • Today

Full-time

USD 185,500.00 - 232,000.00 per year

Programming Manager, Clinical Programming

Genmab

Princeton, New Jersey • Yesterday

Full-time

USD 117,840.00 - 176,760.00 per year

Programming Manager, Clinical Programming

Genmab

Princeton, New Jersey • Yesterday

Full-time

USD 117,840.00 - 176,760.00 per year

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 30 days ago

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New York, New York

•

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

Full-time

USD 213,500.00 - 267,000.00 per year

Senior RAVE Clinical Database Programmer

Remote or New Jersey

•

8d 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

•

Yesterday

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,

Full-time

USD 131,040.00 - 196,560.00 per year

Senior Backend Software Engineer

New York, New York

•

Today

As a Senior Backend Software Engineer on our Diagnostics team, you'll build the part of Regard that reads a patient's medical chart - labs, medications, vitals, procedures, prior notes, history - and determines which conditions are present, along with the evidence supporting each one. You'll design and develop critical backend services and drive them end-to-end through the full product lifecycle: ideation, planning, design, execution, deployment, and iteration. Our senior engineers are true tec

Full-time

USD 175,000.00 - 230,000.00 per year