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Medidata Rave Developer Jobs (NOW HIRING)

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 ...

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 ...

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 ...

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 ...

Sr Mgr EDC Development

Armonk, NY · On-site

$134.40K - $219.20K/yr

Preferred qualifications include Medidata Builder Certification , C# programming knowledge, and TrialGrid familiarity, plus experience with Rave Amendment Manager and Medidata Cloud Administration.

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 ...

Sr Mgr EDC Development

Warren, MI · On-site

$134.40K - $219.20K/yr

Preferred qualifications include Medidata Builder Certification , C# programming knowledge, and TrialGrid familiarity, plus experience with Rave Amendment Manager and Medidata Cloud Administration.

... Medidata Rave, Microsoft Access, and SQL-based systems. A thorough understanding of data integrity, secure data handling, and compliance with Good Clinical Practice (GCP) is essential. This role also ...

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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Medidata Rave Developer information

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How much do medidata rave developer jobs pay per hour?

As of Jun 3, 2026, the average hourly pay for medidata rave developer in the United States is $52.84, according to ZipRecruiter salary data. Most workers in this role earn between $40.38 and $64.66 per hour, depending on experience, location, and employer.

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

To thrive as a Medidata Rave Developer, you need a strong background in clinical data management, database programming, and familiarity with clinical trial processes, often supported by a bachelor's degree in life sciences, computer science, or a related field. Proficiency in Medidata Rave EDC, Rave Architect, and understanding of CDISC standards, along with certifications in Medidata Rave, are typically required. Attention to detail, problem-solving skills, and effective communication are essential soft skills for collaborating with clinical teams and ensuring data accuracy. These skills are crucial for building robust clinical trial databases that support regulatory compliance and reliable data collection in clinical research.

What are some common challenges faced by Medidata Rave Developers when customizing EDC studies, and how can they be addressed?

Medidata Rave Developers often encounter challenges related to balancing complex protocol requirements with system limitations, such as creating custom edit checks or integrating third-party data sources. Managing study amendments and maintaining data integrity during mid-study changes can also be demanding. These challenges can be addressed by thorough documentation, close collaboration with study teams and data managers, and leveraging Medidata community resources for best practices. Staying updated on the latest Medidata Rave releases and participating in regular training can also help developers efficiently handle evolving study needs.

What are Medidata Rave Developers?

Medidata Rave Developers are specialized professionals who design, build, and maintain electronic data capture (EDC) systems using Medidata Rave, a leading platform in clinical data management. They are responsible for creating study databases, designing electronic case report forms (eCRFs), programming edit checks, and ensuring compliance with regulatory standards. Their work enables clinical trial data to be collected, validated, and managed efficiently, supporting pharmaceutical and biotech companies in conducting successful clinical studies.

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

AspectMedidata Rave DeveloperClinical Data Coordinator
Primary RoleDesigning, developing, and maintaining electronic data capture (EDC) systems using Medidata RaveManaging and overseeing clinical trial data collection, entry, and quality control
Required SkillsMedidata Rave platform expertise, database management, scripting, and programming skillsData management, clinical trial processes, attention to detail, and communication skills
Work EnvironmentClinical research organizations, pharmaceutical companies, CROsClinical sites, research organizations, pharmaceutical companies

While both roles are involved in clinical data management, Medidata Rave Developers focus on building and maintaining the electronic data capture systems, whereas Clinical Data Coordinators handle data entry, validation, and quality assurance during trials. Both roles are essential in the clinical research process but differ in technical focus and responsibilities.

More about Medidata Rave Developer jobs
Infographic showing various Medidata Rave Developer job openings in the United States as of May 2026, with employment types broken down into 67% Full Time, and 33% Contract. Highlights an 67% In-person, and 33% Remote job distribution, with an average salary of $109,905 per year, or $52.8 per hour.

Contractor

Posted 13 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