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Volunteer Clinical Programmer Medidata Rave Jobs

TechData Service Company LLC

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Medidata Rave | Clinical Programmer (Remote, Full Time)-LC0002

King Of Prussia, PA · Remote

$90K - $150K/yr

  • Medical

  • Dental

  • Retirement

  • PTO

Qualifications: * 5+ years of EDC database build experience for clinical trial. * Experience with Medidata Rave with Medidata certification; Minimum two to three years current database programming ...

EDETEK

Clinical Database Programmer

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Build and configure study databases in Medidata Rave or other eClinical platforms based on protocol ... Collaborate with data managers, clinical teams, programmers, vendors, and sponsors to clarify ...

Fortrea

$80K - $95K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Lead the development and implementation of Clinical solutions to global technical services issues ... Complete assigned work utilizing Medidata Rave or Oracle Inform or other proprietary software ...

Fortrea

Senior Programmer Analyst

Durham, NC · Remote

$80K - $95K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Lead the development and implementation of Clinical solutions to global technical services issues ... Complete assigned work utilizing Medidata Rave or Oracle Inform or other proprietary software ...

Itlearn360

Director, IT at System One Princeton, NJ

Princeton, NJ · On-site

$120 - $150/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Familiar with clinical systems and trial platforms such as CTMS, Medidata RAVE, EDC, and related ... Programming/Platform: .NET, C#, SQL, Oracle, Git. * Cloud: AWS (Aurora or equivalent) migration and ...

Celerion

EDC Developer / Programmer

Veeva CDMS, Medidata RAVE, etc.) * Experience with Veeva EDC and Veeva CDB preferred * Proficient ... clinical systems and data administration * Must be organized, an effective written and oral ...

Celerion

EDC Developer / Programmer

OR · Remote

Veeva CDMS, Medidata RAVE, etc.) * Experience with Veeva EDC and Veeva CDB preferred * Proficient ... clinical systems and data administration * Must be organized, an effective written and oral ...

MapLight Therapeutics

Clinical Data Manager

Burlington, MA · On-site

$145K - $160K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

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 ...

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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 Aug 16, 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?

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 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:

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The most popular types of Clinical Programmer Medidata Rave jobs are:

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Volunteer Clinical Programmer Medidata Rave jobs near you

Medidata Rave | Clinical Programmer (Remote, Full Time)-LC0002

TechData Service Company LLC

King Of Prussia, PA • Remote

$90K - $150K/yr

Full-time

Medical, Dental, Retirement, PTO

Posted 16 days ago

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Job description

Qualifications:

•5+ years of EDC database build experience for clinical trial.

•Experience with Medidata Rave with Medidata certification; Minimum two to three years current database programming experience designing studies and data validation programming in Medidata Rave.

•Is able to write the code at CF from scratch.

•Familiarity with clinical data regulations (GCP, ICH).

•Familiarity with Operational Qualification/Performance Qualification and UAT execution and documentation.

•BS or MS degree in related discipline.

Responsibilities:

•Build and design clinical study trials in Medidata RAVE system.

•Design/create and test clinical databases including forms, folders, matrices, data

dictionaries/code lists, unit dictionaries, edit checks/rules, derivations, custom functions, standard and custom reports.

•Provide programming expertise to support data capture, review, and monitoring for clinical trials.

•Program reports, edit checks, and custom functions based on study protocol requirements.

•Assist with EDC integration with other systems, including but not limited to IRT system, CTMS system and etc.

•Manage external vendor data import and validation.

•Provide technical support as needed for Medidata RAVE and Merative Zelta EDC systems.

•Participate in EDC design requirements development in collaboration with Study Lead Data Manager and the wider study team.

•Support development of and updates of global library objects as appropriate according to best practices and new standards.

•Perform peer review for the studies built by other programmers.

•Maintain all required Clinical Systems study documentation.

•Provide EDC technical support to facilitate study timelines and deliverables.

•Manage timely-quality deliverables for the study teams for assigned protocol/study(s).

TechData is proud to be an equal opportunity workplace and is an affirmative action employer. We are committed to equal employment opportunity regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity or Veteran status.

Company Description

https://quantive.bio/