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Medidata Rave Programmer Jobs in California (NOW HIRING)

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Medidata Rave Programmer information

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$11

$39

$67

How much do medidata rave programmer jobs pay per hour?

As of Aug 17, 2026, the average hourly pay for medidata rave programmer in California is $39.02, according to ZipRecruiter salary data. Most workers in this role earn between $25.38 and $50.77 per hour, depending on experience, location, and employer.

What is a Medidata Rave Programmer?

A Medidata Rave Programmer is responsible for designing, developing, and managing electronic data capture (EDC) systems using Medidata Rave, a widely used clinical trial software. They create study databases, build edit checks, program custom functions, and ensure data integrity for clinical trials. Their role is essential in streamlining data collection, validation, and reporting for regulatory compliance and efficient trial management.

What does a Medidata Rave Programmer do?

As a Medidata Rave Programmer, your daily tasks often involve designing and programming electronic case report forms (eCRFs), managing edit checks, and customizing the study database in the Medidata Rave platform. You'll collaborate closely with clinical data managers, biostatisticians, and other stakeholders to ensure accurate data capture and compliance with study protocols. Routine responsibilities may also include troubleshooting technical issues, validating builds, and supporting user testing. This role offers a balance of independent programming work and teamwork, providing opportunities to contribute directly to successful clinical trials.

What are the key skills and qualifications needed to thrive as a Medidata Rave Programmer?

To thrive as a Medidata Rave Programmer, you need strong programming skills, experience in electronic data capture (EDC) for clinical trials, and a background in life sciences or a related field. Expertise with Medidata Rave software, familiarity with Rave Architect, and knowledge of relevant clinical data standards or CDISC certification are highly valuable. Attention to detail, effective communication, and problem-solving abilities help you excel in both independent and collaborative environments. These skills and qualities ensure accurate database builds, smooth study execution, and successful teamwork within clinical research settings.

What are the most commonly searched types of Medidata Rave Programmer jobs in California?

The most popular types of Medidata Rave Programmer jobs in California are:

What job categories do people searching Medidata Rave Programmer jobs in California look for?

The top searched job categories for Medidata Rave Programmer jobs in California are:

Infographic showing various Medidata Rave Programmer job openings in California as of August 2026, with employment types broken down into 100% Full Time. Highlights an 60% In-person, and 40% Remote job distribution, with an average salary of $81,158 per year, or $39 per hour.

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Posted 3 days ago

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Job description

Responsibilities:
  • Develop, maintain, and execute SAS programs to support external data transfers, including validation against vendor transfer specifications.
  • Generate and maintain Data Review Listings (DRLs) and Study Health Metrics (SHMs) in accordance with study timelines.
  • Perform peer review of DRLs and data reconciliation reports.
  • Monitor automated job logs and resolve issues as needed.
  • Retrieve and post external vendor data using sFTP/FTP clients and vendor portals.
  • Collaborate with data managers, statistical programmers, biostatistics, and clinical operations to support data cleaning and integrity activities.
  • Contribute to the development and maintenance of SAS macro programs and departmental programming standards.
  • Participate in SOP and work instruction development, including program validation and documentation.
  • Provide guidance and support to junior members of the data programming team.

Requirements:
  • Bachelor's or Master's degree in a relevant field or equivalent experience.
  • 7+ years of clinical data programming experience, with a minimum of 5 years in oncology.
  • Hands-on experience across Phase I, II, and III oncology trials.
  • Proficiency in SAS; working knowledge of Medidata Rave, Business Objects, and Crystal Reports.
  • Familiarity with CDISC, 21 CFR Part 11, ICH, and Google Cloud Platform guidelines.
  • Experience with sFTP/FTP tools and vendor data portals.