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Internship Medidata Rave Programmer Jobs (NOW HIRING)

EDETEK

Clinical Database Programmer

Build and configure study databases in Medidata Rave or other eClinical platforms based on protocol ... Edit Check Programming and Validation * Develop and maintain edit checks, derivations, dynamics ...

Fortrea

$80K - $95K/yr

... Report programming or Visual Analytics tools like Spotfire or Tableau. Develop/validate Custom ... Complete assigned work utilizing Medidata Rave or Oracle Inform or other proprietary software ...

Fortrea

Senior Programmer Analyst

Durham, NC · Remote

$80K - $95K/yr

... Report programming or Visual Analytics tools like Spotfire or Tableau. Develop/validate Custom ... Complete assigned work utilizing Medidata Rave or Oracle Inform or other proprietary software ...

Nexa Trials

Data Architect

Austin, TX · On-site

$100 - $130/hr

Proficiency with at least two major EDC platforms (e.g., Medidata Rave, Veeva Vault CDMS, Oracle ... Collaboration with engineering teams in Lahore and QC operations in Dubai * Conference and ...

MediData

Senior Data Scientist

Manhattan, NY · On-site

$114.75 - $153/hr

About the Team Medidata AI organization is building innovative AI products based on the largest ... The AI features developed will power modern clinical trial study design and study conduct with Rave ...

Medidata Solutions

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

As of Aug 16, 2026, the average hourly pay for internship medidata rave programmer in the United States is $39.54, according to ZipRecruiter salary data. Most workers in this role earn between $25.72 and $51.44 per hour, depending on experience, location, and employer.

What does an internship Medidata Rave programmer do?

An Internship Medidata Rave Programmer assists in designing, developing, and maintaining electronic data capture (EDC) systems using Medidata Rave for clinical trials. Their main tasks include programming study databases, building case report forms (CRFs), and ensuring data quality and compliance with regulatory standards. Interns typically work under the supervision of experienced programmers and may also help troubleshoot technical issues, support data validation, and learn about clinical data management processes. This role provides hands-on experience with clinical trial technology and helps interns build foundational skills for a future career in clinical data programming.

What are some typical projects or tasks an internship Medidata Rave programmer might work on?

As an Internship Medidata Rave Programmer, you can expect to assist with building and maintaining electronic case report forms (eCRFs), validating study configurations, and supporting data management teams in clinical trials. You may also help troubleshoot and resolve issues within Medidata Rave, perform quality checks, and contribute to documentation. Collaboration with experienced programmers and data managers is common, providing valuable exposure to real-world clinical data workflows and industry best practices.

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

AspectInternship Medidata Rave ProgrammerClinical Data Coordinator
Required CredentialsBasic knowledge of Medidata Rave, relevant coursework or certificationsDegree in life sciences, healthcare, or related field; often additional certifications
Work EnvironmentInternship setting, often in pharmaceutical or biotech companiesClinical trial sites or sponsor organizations, managing data entry and quality
Industry UsageUsed primarily in clinical data management and EDC system setupUsed in clinical trial data collection, management, and compliance

The Internship Medidata Rave Programmer typically focuses on learning and supporting EDC system setup and data management using Medidata Rave, often as part of an internship program. In contrast, a Clinical Data Coordinator manages data collection, quality control, and compliance during clinical trials. Both roles are essential in clinical research but differ in responsibilities and experience levels.

What are the key skills and qualifications needed to thrive as an internship Medidata Rave programmer?

To thrive as an Internship Medidata Rave Programmer, you need a solid background in computer science or life sciences, familiarity with clinical data management concepts, and basic programming skills. Experience with Medidata Rave EDC platform, clinical trial management systems, and understanding of CDISC standards or certifications like Medidata Rave certification are valuable. Attention to detail, problem-solving abilities, and strong communication skills help you collaborate effectively with clinical teams and ensure data integrity. These skills are essential for supporting efficient, compliant data capture and management in clinical research environments.
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Internship Medidata Rave Programmer jobs near you
Infographic showing various Internship Medidata Rave Programmer job openings in the United States as of August 2026, with employment types broken down into 50% Full Time, and 50% Contract. Highlights an 75% In-person, and 25% Remote job distribution, with an average salary of $82,234 per year, or $39.5 per hour.

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/