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Medidata Rave Edc Programmer Jobs (NOW HIRING)

Senior Programmer, EDC Systems

Waltham, MA · On-site

$143K - $169K/yr

The Senior Programmer for Data Validation supports cross-functional teams such as Statistics, Data ... Familiarity with EDC systems (e.g., Medidata Rave, Veeva Vault) and understanding of eCRF design ...

... Medidata Rave global library standard objects (e.g., eCRF forms, edit checks) to facilitate the creation of study-level databases. * Work with Data Managers and EDC Programmers to implement new or ...

... Medidata Rave global library standard objects (e.g., eCRF forms, edit checks) to facilitate the creation of study-level databases. * Work with Data Managers and EDC Programmers to implement new or ...

... Medidata Rave global library standard objects (e.g., eCRF forms, edit checks) to facilitate the creation of study-level databases. * Work with Data Managers and EDC Programmers to implement new or ...

... Medidata Rave global library standard objects (e.g., eCRF forms, edit checks) to facilitate the creation of study-level databases. * Work with Data Managers and EDC Programmers to implement new or ...

... Medidata Rave global library standard objects (e.g., eCRF forms, edit checks) to facilitate the creation of study-level databases. * Work with Data Managers and EDC Programmers to implement new or ...

... Medidata Rave global library standard objects (e.g., eCRF forms, edit checks) to facilitate the creation of study-level databases. * Work with Data Managers and EDC Programmers to implement new or ...

... Medidata Rave global library standard objects (e.g., eCRF forms, edit checks) to facilitate the creation of study-level databases. * Work with Data Managers and EDC Programmers to implement new or ...

... Medidata Rave global library standard objects (e.g., eCRF forms, edit checks) to facilitate the creation of study-level databases. * Work with Data Managers and EDC Programmers to implement new or ...

... Medidata Rave global library standard objects (e.g., eCRF forms, edit checks) to facilitate the creation of study-level databases. * Work with Data Managers and EDC Programmers to implement new or ...

... Medidata Rave global library standard objects (e.g., eCRF forms, edit checks) to facilitate the creation of study-level databases. * Work with Data Managers and EDC Programmers to implement new or ...

... Medidata Rave global library standard objects (e.g., eCRF forms, edit checks) to facilitate the creation of study-level databases. * Work with Data Managers and EDC Programmers to implement new or ...

... Medidata Rave global library standard objects (e.g., eCRF forms, edit checks) to facilitate the creation of study-level databases. * Work with Data Managers and EDC Programmers to implement new or ...

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Medidata Rave Edc Programmer information

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How much do medidata rave edc programmer jobs pay per hour?

As of Sep 11, 2026, the average hourly pay for medidata rave edc programmer 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 a Medidata Rave EDC programmer?

A Medidata Rave EDC Programmer is a specialist who designs, builds, and manages electronic case report forms (eCRFs) and databases using the Medidata Rave Electronic Data Capture (EDC) system. They play a critical role in clinical trials by ensuring that data collection processes are efficient, compliant, and meet study requirements. Their responsibilities typically include configuring study databases, validating data entry, troubleshooting issues, and supporting study teams throughout the trial lifecycle. These professionals often collaborate with clinical data managers, biostatisticians, and regulatory teams to ensure high-quality clinical data management.

What are some common challenges faced by Medidata Rave EDC programmers during study builds, and how can they be addressed?

Medidata Rave EDC Programmers often encounter challenges such as managing frequent mid-study changes, ensuring data integrity while implementing complex protocol requirements, and coordinating effectively with clinical operations and data management teams. Addressing these challenges requires strong attention to detail, robust documentation practices, and proactive communication with stakeholders to clarify study specifications and timelines. Leveraging Rave's built-in validation tools, thorough user acceptance testing, and continuous training on platform updates can also help mitigate issues and ensure successful study builds.

What are the key skills and qualifications needed to thrive as a Medidata Rave EDC programmer, and why are they important?

To thrive as a Medidata Rave EDC Programmer, you need strong expertise in electronic data capture (EDC) systems, clinical data management, and a background in life sciences or computer science. Familiarity with Medidata Rave, Rave Architect, and programming languages such as SQL or SAS, along with Medidata certifications, are typically required. Attention to detail, problem-solving abilities, and effective communication set standout professionals apart in this role. These skills ensure accurate data capture, regulatory compliance, and smooth collaboration across clinical research teams.

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

AspectMedidata Rave Edc ProgrammerClinical Data Coordinator
Primary RoleDesigns and develops electronic data capture (EDC) systems using Medidata RaveManages and oversees data collection, entry, and quality in clinical trials
Required SkillsProficiency in Medidata Rave, database management, programming, and clinical trial processesData management, attention to detail, communication, and knowledge of clinical protocols
Work EnvironmentClinical research organizations, pharmaceutical companies, CROsClinical sites, research organizations, pharmaceutical companies

While both roles involve clinical data, the Medidata Rave Edc Programmer focuses on developing and maintaining electronic data capture systems, whereas the Clinical Data Coordinator manages data entry and quality assurance during trials. The programmer requires technical skills in Medidata Rave, while the coordinator emphasizes data management and communication skills.

What are popular job titles related to Medidata Rave Edc Programmer jobs?

For Medidata Rave Edc Programmer jobs, the most frequently searched job titles are:

Infographic showing various Medidata Rave Edc Programmer job openings in the United States as of September 2026, with employment types broken down into 89% Full Time, 3% Part Time, 7% Contract, and 1% Nights. Highlights an 89% Physical, 2% Hybrid, and 9% Remote job distribution, with an average salary of $134,731 per year, or $64.8 per hour.

Medidata Rave Programmer (Remote)-LC0003-late-phase and FIH studies

San Diego, CA • Remote

TechData Service Company LLC
Biotechnology Research and Development • 51 - 200 employees

$90K - $150K/yr

Temporary

Medical, Dental

Posted 7 days ago

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Job description

Qualifications:

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

Has experience building databases for late-phase and FIH studies in Medidata Rave EDC.

•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/