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Internship Medidata Rave Programmer Jobs (NOW HIRING)

Atorus Research

Sr Medidata RAVE Programmer

Sr Medidata RAVE Programmer Remote from anywhere in the U.S. or Canada Contract/Corp to Corp JOB OVERVIEW The Electronic Data Capture (EDC) Programmer is responsible for providing support in creating ...

SystImmune Inc.

EDC Programmer

Redmond, WA · On-site

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

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 ...

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 ...

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 ...

Immunome, Inc.

SeniorEDC Programmer

Bothell, WA · On-site

Position Overview The Senior EDC (Electronic Data Capture) Programmer (Sr. EDCP) is responsible for ... Strong hands-on experience with at least one major EDC platform (Medidata Rave preferred). * Solid ...

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

As of Jun 29, 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, and why are they important?

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 June 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.

Sr Medidata RAVE Programmer

Atorus Research

Remote

Contractor

Posted 8 days ago

Job description

Sr Medidata RAVE Programmer
Remote from anywhere in the U.S. or Canada
Contract/Corp to Corp
JOB OVERVIEW
The Electronic Data Capture (EDC) Programmer is responsible for providing support in creating, deploying and maintaining clinical databases and provides EDC programming support to the study team in accordance with Atorus and/or sponsor standard operating procedures (SOPs), Good Clinical Practice (GCP), ICH Guidelines and sponsor requirements. The EDC Programmer also assists in technical support for data collection systems.
JOB RESPONSIBILITIES
• Perform study set up and program edit check programming as per the approved specifications with minimal guidance from the line manager or experienced colleagues
• Adhere to project timelines
• Participate in the design and maintenance of the clinical study database per the protocol and any amendments, SOPs, GCP and other regulatory requirements
• Review database specifications and Data Validation Specifications (DVS) and perform programming and configuration activities
• Assist in database release to production activities
• Provide programming or other support and assist CDM managers in daily technical operations. Respond to and solve technical oriented problems in a timely manner, as appropriate for the position. Assist data manager with status reports and listings as necessary
• Advise management on a regular basis on the status and any potential risks or concerns with ongoing projects to ensure timely resolution including any potential issues with resources
• Ensure awareness of project-specific quality and performance standards and ensure that these are adequately documented, communicated, and understood
• Participate in internal and external study team meetings, as required
• Participate in department meetings and initiatives
• Perform other duties as required by the department
QUALIFICATIONS AND EDUCATION REQUIREMENTS
• University/college degree (life science, pharmacy or related subject preferred), or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing certification, medical or laboratory technology)
• 2-4years EDC Programming experience working in pharmaceutical, biotechnology or Contract Research Organization (CRO) preferred
• Course completion of an EDC system training
• Minimum 2-4 years of experience in clinical database design and deployment
• Additional relevant work experience will be considered in lieu of formal qualifications
• Broad knowledge of drug development processes
• Understanding of global clinical development budgets and relationship to productivity targets
• Knowledge of effective clinical data management practices
PREFERRED SKILLS
• Good organizational skills
• Good communication skills, verbal and written
• Detail oriented
• Good computer skills, including Microsoft Office and use of data management systems
• Good problem-solving skills
• Basic knowledge and understanding of EDC and other eTechnologies
• Flexible, team player
• Proven ability to organize and effectively prioritize workload and deliverables

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