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Volunteer Clinical Programmer Medidata Rave Jobs

CTI

Clinical Programmer

Covington, KY · On-site +1

A Clinical Programmer will support the design, development, and validation of clinical trial ... In this role, you will build and test study databases using platforms such as Medidata Rave or ...

Atorus Research

Sr Medidata RAVE Programmer

Sr Medidata RAVE Programmer Remote from anywhere in the U.S. or Canada Contract/Corp to Corp JOB ... and maintaining clinical databases and provides EDC programming support to the study team in ...

CTI

Clinical Programmer

Covington, KY · On-site +1

A Clinical Programmer will support the design, development, and validation of clinical trial ... In this role, you will build and test study databases using platforms such as Medidata Rave or ...

Systimmune

EDC Programmer

Redmond, WA · On-site

$100K - $150K/yr

Design and build Medidata Rave studies from the ground up across Phase I, II, and III clinical trials, including eCRF design, edit check programming, and study configuration. * Develop custom ...

SystImmune, Inc

EDC Programmer

Redmond, WA · On-site

$100K - $150K/yr

Design and build Medidata Rave studies from the ground up across Phase I, II, and III clinical trials, including eCRF design, edit check programming, and study configuration. * Develop custom ...

Cytel

Senior Database Developer

Cambridge, MA · On-site +1

At least 8 years progressive Clinical Research Experience * Medidata Rave Certified Study Builder * 6 years' experience as a database programmer * Bachelor's degree Required

Cytel

Senior Database Developer

Cambridge, MA · On-site +1

At least 8 years progressive Clinical Research Experience * Medidata Rave Certified Study Builder * 6 years' experience as a database programmer * Bachelor's degree Required

Immunome, Inc.

SeniorEDC Programmer

Bothell, WA

Position Overview The Senior EDC (Electronic Data Capture) Programmer (Sr. EDCP) is responsible for ... Medidata Rave preferred). * Solid understanding of clinical trial processes and data flow.

Cytel

Senior Clinical Programmer

Cambridge, MA · On-site +1

The ideal candidate will have 4-6 years of experience in clinical data programming, with a focus on clinical trial systems and data management solutions especially RAVE and Elluminate. This position ...

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All JobsVolunteer Clinical Programmer Medidata Rave Jobs

Volunteer Clinical Programmer Medidata Rave information

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How much do volunteer clinical programmer medidata rave jobs pay per hour?

As of Jun 9, 2026, the average hourly pay for volunteer clinical programmer medidata rave in the United States is $64.77, according to ZipRecruiter salary data. Most workers in this role earn between $53.61 and $73.32 per hour, depending on experience, location, and employer.

What is the difference between Volunteer Clinical Programmer Medidata Rave vs Clinical Data Coordinator?

AspectVolunteer Clinical Programmer Medidata RaveClinical Data Coordinator
CredentialsBasic programming knowledge, familiarity with Medidata RaveDegree in health sciences or related field, data management experience
Work EnvironmentClinical trial data management, using Medidata Rave softwareData collection, entry, and quality control in clinical settings
Employer & IndustryPharmaceutical companies, CROs, biotech firmsHospitals, research institutions, clinical trial sites

The Volunteer Clinical Programmer Medidata Rave primarily focuses on configuring and managing clinical trial data within the Medidata Rave platform, often on a volunteer basis. In contrast, a Clinical Data Coordinator handles broader data management tasks, including data entry, validation, and quality assurance. While both roles require knowledge of clinical data processes, the Programmer role emphasizes technical software skills, whereas the Coordinator role involves more administrative and oversight responsibilities.

What are the key skills and qualifications needed to thrive as a Volunteer Clinical Programmer Medidata Rave, and why are they important?

To thrive as a Volunteer Clinical Programmer Medidata Rave, you need a solid understanding of clinical data management, programming principles (such as SQL or SAS), and familiarity with clinical trial processes, often supported by a degree in life sciences, computer science, or a related field. Proficiency with Medidata Rave EDC systems, CRF design, and data validation tools, as well as knowledge of CDISC standards, are typically required. Attention to detail, problem-solving ability, and strong communication skills help ensure data integrity and effective collaboration with study teams. These competencies are crucial for delivering accurate, compliant clinical data that support successful clinical trial outcomes.

What is a Volunteer Clinical Programmer Medidata Rave?

A Volunteer Clinical Programmer Medidata Rave is an individual who assists with programming tasks related to clinical trials using the Medidata Rave electronic data capture (EDC) system, typically on a volunteer or unpaid basis. Their main responsibilities include designing and building electronic case report forms (eCRFs), programming edit checks, and ensuring data integrity within the Rave platform. They work closely with clinical data managers and study teams to support the accurate and efficient collection of clinical trial data. This role is ideal for those seeking to gain experience in clinical data management and clinical programming, especially with the widely used Medidata Rave system.

What are some common challenges faced by a Volunteer Clinical Programmer working with Medidata Rave, and how can they be addressed?

Volunteer Clinical Programmers using Medidata Rave often face challenges such as adapting to strict data standards, managing complex study protocols, and ensuring data quality within tight timelines. Since volunteers may have limited prior exposure to the organization's specific workflows, familiarizing yourself with Medidata Rave's interface and standard operating procedures is crucial. Collaborating closely with clinical data managers and IT teams can help resolve data discrepancies quickly and ensure compliance with regulatory requirements. Proactively seeking training resources and participating in team meetings will help you stay aligned with project goals and improve your technical proficiency.
What cities are hiring for Volunteer Clinical Programmer Medidata Rave jobs? Cities with the most Volunteer Clinical Programmer Medidata Rave job openings:
What are the most commonly searched types of Clinical Programmer Medidata Rave jobs? The most popular types of Clinical Programmer Medidata Rave jobs are:
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Volunteer Clinical Programmer Medidata Rave jobs near you

Clinical Development Engineer (Medidata Rave / Technical Support)

Group Nine LLC

Passaic, NJ

Other

Posted 2 days 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.

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