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Entry Level Medidata Rave Programmer Jobs (NOW HIRING)

MiniMed

Sr Clinical IT Developer

... Medidata Rave and or other (Veeva EDC or Oracle EDC or other smaller systems) and clinical trial ... May provide guidance and assistance to entry level professionals and / or employee in Support ...

MiniMed

Sr Clinical IT Developer

Los Angeles, CA · On-site

... Medidata Rave and or other (Veeva EDC or Oracle EDC or other smaller systems) and clinical trial ... May provide guidance and assistance to entry level professionals and / or employee in Support ...

RTI International

Applications Systems Analyst

... programming languages and methodologies, including .NET, Java, TypeScript/JavaScript, and Python. * Familiarity with Electronic Data Capture (EDC) systems such as Medidata RAVE, or REDCap. * Some ...

Everest Clinical Research Services Inc.

One year clinical database design experience, such as developing clinical databases in DFdiscover, InForm, Medidata Rave, Clinical One, and/or other EDC systems. * Software programming experience ...

Everest Clinical Research

Clinical Database Designer I

$50K - $90K/yr

One year clinical database design experience, such as developing clinical databases in DFdiscover, InForm, Medidata Rave, Clinical One, and/or other EDC systems. * Software programming experience ...

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Entry Level Medidata Rave Programmer information

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How much do entry level medidata rave programmer jobs pay per hour?

As of Sep 11, 2026, the average hourly pay for entry level medidata rave programmer in the United States is $26.73, according to ZipRecruiter salary data. Most workers in this role earn between $17.07 and $23.08 per hour, depending on experience, location, and employer.

What is an entry level Medidata Rave programmer?

An Entry Level Medidata Rave Programmer is a professional who works with the Medidata Rave electronic data capture (EDC) system, primarily used in clinical research for managing and processing clinical trial data. They are responsible for programming study builds, designing electronic case report forms (eCRFs), and ensuring data integrity within the Rave platform. Typically, entry-level programmers collaborate with data managers and clinical teams to support study setup, validation, and troubleshooting. This role often requires knowledge of clinical data standards and some experience with programming or database management.

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

To thrive as an Entry Level Medidata Rave Programmer, you need a solid understanding of clinical data management concepts, basic programming or database skills, and a relevant degree in life sciences, computer science, or a related field. Familiarity with Medidata Rave EDC, SQL, and possibly certifications in Medidata Rave or clinical data management tools are typically required. Attention to detail, problem-solving abilities, and effective communication help you collaborate with clinical teams and ensure data accuracy. These skills ensure the integrity of clinical trial data, regulatory compliance, and efficient study execution.

What are some common challenges faced by entry level Medidata Rave programmers, and how can they be overcome?

Entry-level Medidata Rave Programmers often encounter challenges such as learning the intricacies of the Rave EDC platform, understanding clinical trial protocols, and managing data validation logic. Adapting to the highly regulated environment of clinical research can also be demanding. Overcoming these challenges involves proactive learning through available Medidata training resources, seeking mentorship from experienced colleagues, and consistently practicing configuration and testing within the system. Collaborating closely with data managers and clinical teams helps clarify requirements and ensures high-quality data capture.

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

AspectEntry Level Medidata Rave ProgrammerClinical Data Coordinator
Required CredentialsBachelor's in Life Sciences, basic Medidata Rave knowledgeBachelor's in Health Sciences, data management experience
Work EnvironmentClinical trial data management teams, CROs, pharmaceutical companiesClinical sites, research organizations, CROs
Employer & Industry UsageUsed for electronic data capture and database setupOversees data collection, quality, and compliance

Entry Level Medidata Rave Programmers focus on configuring and managing electronic data capture systems, while Clinical Data Coordinators handle data collection, quality control, and compliance at clinical sites. Both roles are essential in clinical trials but differ in responsibilities and daily tasks.

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Entry Level Medidata Rave Programmer jobs near you
Infographic showing various Entry Level Medidata Rave Programmer job openings in the United States as of September 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $55,594 per year, or $26.7 per hour.

CDM Programmer II - Medidata Rave

Wilmington, NC • On-site

Ruri Software Technologies LLC
Software Development • 11 - 50 employees
Learn more about Ruri Software Technologies LLCexternal

Full-time

Re-posted 24 days ago

Job description

Title: CDM Programmer II - Medidata Rave
Location: Wilmington, NC, United States
Description:
Note:
Skill set required is RAVE, edit check expertise/customs function programming. BELT experience, protocol amendment or maintenance. RAVE migrations, etc. Very strong communication skills. remote anywhere in the US
Database position working with clinical trials data systems under general supervision. Provides technical leadership for some or all of the following activities: Designs and implements global library and study specific setup for clinical trials applications; develops and validates data checks; provides first-line enduser support/problem solving; provides support for application validation activities.
• Serves as Technical Lead on Study specific database design / build activities adhering to the timelines established by the project team and indicated by the contract.
• Reviews designs for compliance/feasibility within the database system and consistency with any current standards and/or sponsor specification and meets with study teams on a regular basis during initial study setup to ensure effective communication and accuracy in design
• Develops and validates data checks and performs core setup and supports processes for various peripheral systems
• Coordinates the activities of other Database Programmers that might assist in building studies to ensure all jobs are carried out and timelines are met.
• Updates annotations and production databases where required based on protocol amendments or other changes to trial designs within timelines as agreed with project team
• Provides basic technical support / consultancy and end-user support
• Works with IT in troubleshooting, reporting and resolving system issues
Minimum Required Education and Experience:
Bachelor's degree in computer science, statistics, biostatistics, mathematics, biology or other
health related field or equivalent experience that provides the skills and knowledge necessary to
perform the job.
Minimum of 2 years experience in a clinical trials environment or similar field
Minimum of 1 years experience with Oracle or similar applications in a programming or
administration capacity. OC/RDC experience preferred.
Minimum of 1 year experience with Medidata Rave and/or Rave certification
Required Knowledge, Skills and Abilities:
Good organizational skills with the ability to adapt and adjust to changing priorities and to manage multiple assignments with challenging/conflicting deadlines.
Good computer skills
Knowledge of relational database systems (RDBMS) and structure
Experience in Oracle and with Oracle tools or similar, with working knowledge of SQL and/or PLSQL
Strong attention to detail and problem solving skills
Good written and verbal communication skills
Demonstrated experience in identification and resolution of technical problems in a professional environment
Ability to maintain a high degree of confidentiality with clinical data and client's proprietary data
Ability to attain, maintain and apply a working knowledge of GCPs and applicable SOPs
Demonstrated positive attitude, enthusiasm toward work, and the ability to work well with others.

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