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Medidata Rave Developer Jobs (NOW HIRING)

The SDTM (Study Data Tabulation Model) Specialist is part of the ACTG and IMPAACT Medidata Rave ... Work directly with the statistician and programmer who is responsible for the ADaM datasets Reports ...

New

As an EDC Database Developer, you will build and administer EDC trials for client contracted ... Veeva CDMS, Medidata RAVE, etc.) * Experience with Veeva EDC and Veeva CDB preferred * Proficient ...

Senior EDC Programmer

Bothell, WA ยท On-site

$115K - $150K/yr

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 ...

As an EDC Database Developer, you will build and administer EDC trials for client contracted ... Veeva CDMS, Medidata RAVE, etc.) * Experience with Veeva EDC and Veeva CDB preferred * Proficient ...

Senior Clinical Data Manager

Cambridge, MA ยท On-site

$144K - $167K/yr

Work with DB programmers to design (e)CRFs and edit checks in EDC system for complex studies * Lead ... Expertise with EDC systems, such as Medidata Rave, InForm, Medrio * Excellent organizational and ...

... Medidata Product and Engineering teams. * Change Management: Guide clinical trial sites and ... products beyond Rave or CTMS. * Audit & Compliance Readiness: Ability to maintain meticulous ...

Clinical Research Nurse

Philadelphia, PA ยท Hybrid

$40 - $45/hr

Experience with electronic data capture (EDC) systems such as Inform and MediData Rave. * Strong ... About Actalent Actalent is a global leader in engineering and sciences services and talent ...

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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 24, 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 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 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 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.

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.
More about Medidata Rave Developer jobs
Infographic showing various Medidata Rave Developer job openings in the United States as of June 2026, with employment types broken down into 1% Internship, 2% Full Time, 1% Part Time, 2% Temporary, and 94% Contract. Highlights an 81% Physical, 5% Hybrid, and 14% Remote job distribution, with an average salary of $109,905 per year, or $52.8 per hour.

LIMS ,Pharma Sr. Business Analyst/Product Owner(San Francisco, CA) Onsite day 1

TestingXperts Inc. DBA Damcosoft

San Francisco, CA โ€ข On-site

$109K - $140K/yr

Contractor

Posted 8 days ago


Job description

LIMS ,Pharma Sr. Business Analyst/Product Owner(San Francisco, CA) Onsite

Pharma R&D Functional Expert

Location: San Francisco, CA โ€“ Onsite
Type: Contract

We are looking to engage an experienced Pharma R&D Functional Expert for one of our clients in San Francisco.

Role Overview:
The consultant will serve as the primary contact for the development of a data and analytics platform on Databricks, acting as the bridge between customerโ€™s R&D stakeholders and the technical data engineering team. The key responsibility will be to define business rules/logic and provide clear documentation for implementation.

Key Requirements:

  • 8โ€“10 years of experience in the pharmaceutical/biotech industry, specifically in R&D, clinical operations, or bioinformatics data management.
  • Strong communication skills to translate scientific/clinical requirements into technical specifications.
  • Experience with clinical data systems (Medidata RAVE or other EDC platforms).
  • Familiarity with CDISC standards (SDTM, ADaM) and LIMS.
  • Good understanding of clinical trial processes.

Nice to Have:

  • Exposure to genomics data (NGS, gnomAD, GWAS) and bioinformatics data lifecycle.
  • Knowledge of SAS and R in statistical/clinical reporting and regulatory submissions.
  • Experience with data platforms (data lakes, data mesh), cloud (Azure preferred), and Databricks/Spark.
  • Translational medicine experience.

Thanks and Regards,

Rajiv Kumar

Associate Manager

Corporate Office:ย  650 Wilson Lane, Suite 201, Mechanicsburg, PA 17055

Testingxperts Inc DBA Damcosoft

P: +1 631-759-8044ย  Ext 518

E:ย Rajiv.kumar@damcosoft.comย ย 

https://www.linkedin.com/in/rajiv-kumar-38396310a/