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Medidata Rave Jobs in Edison, NJ (NOW HIRING)

Medidata Rave global library standard objects (e.g., eCRF forms, edit checks). * Build, maintain, and document the Medidata Rave global library standard objects (e.g., eCRF forms, edit checks) to ...

Medidata Rave global library standard objects (e.g., eCRF forms, edit checks). * Build, maintain, and document the Medidata Rave global library standard objects (e.g., eCRF forms, edit checks) to ...

Medidata Rave global library standard objects (e.g., eCRF forms, edit checks). * Build, maintain, and document the Medidata Rave global library standard objects (e.g., eCRF forms, edit checks) to ...

Medidata Rave global library standard objects (e.g., eCRF forms, edit checks). * Build, maintain, and document the Medidata Rave global library standard objects (e.g., eCRF forms, edit checks) to ...

Senior Data Scientist

New York, NY · On-site

$114K - $153K/yr

Medidata is powering smarter treatments and healthier people through digital solutions to support ... The AI features developed will power modern clinical trial study design and study conduct with Rave ...

Expertise with Medidata Rave, Oracle InForm, or similar EDC systems. * Strong understanding of GCP, ICH, and clinical research processes. * Excellent communication and leadership skills. * An ...

Expertise with Medidata Rave, Oracle InForm, or similar EDC systems. * Strong understanding of GCP, ICH, and clinical research processes. * Excellent communication and leadership skills. * An ...

Expertise with Medidata Rave, Oracle InForm, or similar EDC systems. * Strong understanding of GCP, ICH, and clinical research processes. * Excellent communication and leadership skills. * An ...

Expertise with Medidata Rave, Oracle InForm, or similar EDC systems. * Strong understanding of GCP, ICH, and clinical research processes. * Excellent communication and leadership skills. * An ...

Senior Data Scientist

New York, NY · On-site

$114K - $153K/yr

Medidata is powering smarter treatments and healthier people through digital solutions to support ... The AI features developed will power modern clinical trial study design and study conduct with Rave ...

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Medidata Rave information

What is a Medidata Rave?

A Medidata Rave job typically involves working with Medidata Rave, a widely used electronic data capture (EDC) system in clinical trials. Professionals in this role manage study databases, design case report forms (CRFs), ensure data integrity, and support clinical research teams. Roles may include Rave Study Builder, Data Manager, or Clinical Programmer. Strong knowledge of clinical trial processes, database management, and SQL is often required.

What are the key skills and qualifications needed to thrive in the Medidata Rave position, and why are they important?

To thrive as a Medidata Rave specialist, you need a solid understanding of Electronic Data Capture (EDC) systems, clinical data management, and regulatory guidelines, typically supported by certifications in Medidata Rave or relevant clinical research fields. Proficiency with the Medidata Rave platform, user administration, and familiarity with tools such as SQL or other database management systems are highly valued. Strong attention to detail, communication, and problem-solving skills help professionals stand out in this role. These qualities ensure accurate data collection, regulatory compliance, and effective collaboration in complex clinical trial environments.

What are some common challenges faced by Medidata Rave specialists in clinical trials?

Medidata Rave specialists often encounter challenges such as ensuring data accuracy across multiple sites, managing complex study protocols, and troubleshooting technical issues within the platform. They are responsible for configuring case report forms, supporting site users, and maintaining regulatory compliance, which requires constant vigilance and adaptability. Collaboration with clinical research teams, sponsors, and IT staff is vital to address study-specific needs and resolve problems efficiently. These challenges make the role dynamic but also provide opportunities for continuous learning and professional growth.

Infographic showing various Medidata Rave job openings in Edison, NJ as of July 2026, with employment types broken down into 58% Full Time, and 42% Contract. Highlights an 100% In-person job distribution.

Clinical Development Engineer (Medidata Rave / Technical Support)

Group Nine LLC

Passaic, NJ • On-site

Other

Re-posted 11 hours ago


Job description

Clinical Development Engineer (Medidata Rave / Technical Support)

We are seeking a Clinical Development Support Engineer with deep technical expertise in Medidata Rave and related clinical data systems. The role involves supporting critical applications across the Clinical Development lifecycle, managing integrations, automations, and troubleshooting technical issues across application, database, and interface layers. The ideal candidate will possess a mix of domain knowledge in Life Sciences and strong technical capabilities in SQL, Python, API integrations, and modern DevOps/automation tools.

Key Responsibilities
  • Provide technical and functional support for Medidata Rave, including database-level analysis, configuration, user management, and issue resolution.
  • Conduct advanced troubleshooting and root cause analysis for incidents, service requests, and integrations across the Clinical Development ecosystem.
  • Manage support operations and ticket workflows using ServiceNow, ensuring adherence to SLAs and documentation best practices.
  • Develop, optimize, and maintain SQL scripts and stored procedures in Microsoft SQL Server for reporting, validation, and data migration.
  • Create and maintain Python scripts for automation, RPA support, and ad-hoc data processing.
  • Work with RESTful APIs for integration, authentication, and data exchange between systems.
  • Support Java-based authentication utilities (JAR files) and assist in integration troubleshooting.
  • Design dashboards and reports using Tableau to support operational and analytical reporting.
  • Perform data analysis and transformation using SAS for clinical and operational datasets.
  • Utilize Git and Bitbucket for version control and code collaboration.
  • Use Atlassian tools (Jira, Confluence, Bitbucket) for task management, documentation, and collaboration across teams.
  • Manage cron-based automation schedules using VisualCron and perform basic MS-DOS command line operations for log reviews and file management.
  • Participate in validation, change management, and release activities ensuring compliance with GxP and 21 CFR Part 11.
  • Document configurations, workflows, troubleshooting steps, and reusable scripts in Confluence or standard knowledge repositories.
Nice to Have
  • SQL (Advanced–Expert): Complex query writing, joins, and performance optimization.
  • Microsoft SQL Server (Intermediate): Stored procedures and database management.
  • Python (Intermediate): Automation scripting, RPA, and data manipulation.
  • Java (Basic): Working knowledge of authentication modules and JAR handling.
  • REST API (Intermediate): Integration, data exchange, and debugging experience.
  • Tableau (Intermediate): Dashboard and visualization development.
  • SAS (Intermediate): Statistical or operational data analysis and reporting.
  • Git (Intermediate): Branching, merging, and code version management.
  • Atlassian Suite (Intermediate): Jira (task tracking), Confluence (documentation), Bitbucket (source control).
  • VisualCron (Basic): Job scheduling, monitoring, and automation setup.
  • MS-DOS Command Line (Basic): File navigation, scripting, and log handling.
  • Experience with ServiceNow or equivalent ITSM/ticketing system.
Required Skills & Qualifications
  • Bachelor's degree in Computer Science, Life Sciences, Bioinformatics, or related discipline.
  • 4–8 years of experience in Clinical Development or Clinical Data Systems support.
  • Strong hands-on experience with Medidata Rave (front-end and back-end).
  • Excellent troubleshooting and root cause analysis skills across application and data layers.
  • Strong communication, documentation, and cross-functional collaboration skills.
Preferred Qualifications
  • Prior experience in pharmaceutical R&D or clinical data management environments.
  • Familiarity with GxP, 21 CFR Part 11, and other regulatory frameworks.
  • Exposure to cloud platforms and integration monitoring tools.
  • Experience with data visualization and automation initiatives supporting clinical operations.