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Freelance Clinical Programmer Medidata Rave Jobs

Atorus Research

Sr Medidata RAVE Programmer

Sr Medidata RAVE Programmer Remote from anywhere in the U.S. or Canada Contract/Corp to Corp JOB ... and maintaining clinical databases and provides EDC programming support to the study team in ...

EDETEK

Clinical Database Programmer

Build and configure study databases in Medidata Rave or other eClinical platforms based on protocol ... Collaborate with data managers, clinical teams, programmers, vendors, and sponsors to clarify ...

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 ...

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How much do freelance clinical programmer medidata rave jobs pay per hour?

As of Jul 22, 2026, the average hourly pay for freelance clinical programmer medidata rave in the United States is $64.77, according to ZipRecruiter salary data. Most workers in this role earn between $53.61 and $73.32 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Freelance Clinical Programmer specializing in Medidata Rave, and why are they important?

To excel as a Freelance Clinical Programmer Medidata Rave, you need a solid understanding of clinical data management, database design, and programming—often backed by a degree in life sciences, computer science, or a related field. Expertise in Medidata Rave EDC, CDISC standards (SDTM, CDASH), and relevant programming languages like SQL or SAS is typically required, along with certifications in Medidata Rave. Strong attention to detail, problem-solving abilities, and effective communication with cross-functional teams are vital soft skills. These competencies ensure efficient, compliant clinical trial data handling and facilitate seamless collaboration in a highly regulated environment.

What does a Freelance Clinical Programmer specializing in Medidata Rave do?

A Freelance Clinical Programmer with expertise in Medidata Rave is responsible for designing, programming, and maintaining electronic data capture (EDC) systems for clinical trials using the Medidata Rave platform. Their tasks include building and validating study databases, creating eCRFs (electronic Case Report Forms), programming edit checks, and ensuring data integrity and compliance with regulatory standards. As freelancers, they typically work on a contract basis for pharmaceutical companies, CROs, or research organizations, and must stay updated on both industry regulations and the latest Medidata Rave functionalities.

What are some typical challenges a Freelance Clinical Programmer faces when working with Medidata Rave, and how can they be managed?

Freelance Clinical Programmers working with Medidata Rave often encounter challenges such as understanding complex study protocols, handling tight timelines, and ensuring accurate data mapping across multiple studies. Since freelancers may not have immediate access to on-site teams, effective remote communication and documentation are crucial for resolving queries with data managers and sponsors. Staying updated with Medidata Rave's latest features and maintaining strong organizational skills can help manage these challenges efficiently and deliver high-quality results.
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Freelance Clinical Programmer Medidata Rave jobs near you
Infographic showing various Freelance Clinical Programmer Medidata Rave job openings in the United States as of July 2026, with employment types broken down into 75% Full Time, and 25% Contract. Highlights an 75% In-person, 3% Hybrid, and 22% Remote job distribution, with an average salary of $134,731 per year, or $64.8 per hour.
CDM Programmer II - Medidata Rave

CDM Programmer II - Medidata Rave

Ruri Software Technologies LLC

Wilmington, NC • On-site

Full-time

This job post has expired today. Applications are no longer accepted.

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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