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Volunteer Clinical Programmer Medidata Rave Jobs

MapLight Therapeutics

Clinical Data Manager

Burlington, MA · On-site

$145K - $160K/yr

MapLight Therapeutics is a clinical stage biotech company that focuses on drug discovery for ... Oversee Medidata Rave electronic data capture (EDC) system setup, configuration, user management ...

Veristat

Senior Clinical Database Programmer The Senior Clinical Database Programmer will work under the ... Medidata Rave, Oracle InForm/ Central Designer, Veeva, DataLabs, Medrio. 4 years' experience ...

Mercor

Biotech Specialist - AI Trainer

Houston, TX · On-site +1

$1.1K - $1.4K/wk

Build a realistic digital workspace using tools like Medidata Rave , Oracle Clinical One , Schrödinger Suite , and Benchling . Include study protocols, IND/NDA/BLA drafts, and lab notebooks.

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Volunteer Clinical Programmer Medidata Rave information

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

As of Jul 6, 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.
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Volunteer Clinical Programmer Medidata Rave jobs near you
Sr Manager Standards & Systems

Sr Manager Standards & Systems

System One

Plainsboro, NJ • Remote

Contractor

Medical, Dental, Vision, Life, Retirement

Posted 19 days ago

Job description

Job Title: Sr Manager Standards & Systems Location: REMOTE Hours: 40.0

Overview

Responsibilities

  • Serve as the primary point of contact for activities related to “Rave Safety Gateway” implementation, developing, testing, and implementing complex edit checks and custom functions to support setup and integration.
  • Translate clinical and safety business requirements into efficient, structured programming logic.
  • Develop and maintain high-quality, reusable programming components to enhance the Genmab Global Library in compliance with data standards, processes, and governance.
  • Create VBA solutions for data validation and reconciliation across multiple Excel sheets to ensure accuracy, consistency, and compliance.
  • Validate Medidata Rave Safety Gateway (RSG) implementation components, ensuring alignment with specifications and data consistency.
  • Manage deliverables and coordinate with internal and external partners throughout the RSG implementation lifecycle.
  • Configure and maintain Rave Safety Gateway modules, including AE data flow and E2B format compatibility.
  • Develop and validate RSG Custom Functions (C#), and contribute to workflow definitions, troubleshooting, and system configuration.
  • Support development and updates for the Genmab Global CRF Library (GLIB), including form reuse, standard objects, and edit checks.
  • Perform cross-sheet validation, generate QC reports, and implement business rule checks in Excel VBA tools.
  • Own project deliverables, managing timelines, risks, issues, and stakeholder communications effectively.

Requirements

  • Bachelor’s degree or equivalent experience in a relevant field.
  • Experience configuring and maintaining Medidata Rave Safety Gateway modules and workflows.
  • Strong Excel VBA programming skills, with proven experience in data validation and reconciliation.
  • Deep understanding of RSG custom functions (C#) programming and deployment.
  • Experience developing and maintaining Genmab Global CRF Library assets and standards.
  • Ability to troubleshoot, monitor, and optimize RSG logic across study phases.
  • Excellent stakeholder management, communication, and documentation skills.
  • Knowledge of E2B data formats and safety data flow processes.
  • Ability to work independently, manage multiple priorities, and meet deadlines in a fast-paced environment.

System One, and its subsidiaries including Joulé and Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan.

System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law.

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Ref: #568-Clinical

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