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Clinical Programmer Medidata Rave Jobs (NOW HIRING)

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 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 ...

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 ...

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 ...

Apply Early

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 ...

Sr. Clinical Programmer Syneos Health is a leading fully-integrated life sciences services ... Utilizes primary development tools including Medidata, Rave, Oracle OC/RDC, Oracle Inform, and/or ...

Sr. Clinical Programmer Syneos Health is a leading fully-integrated life sciences services ... Utilizes primary development tools including Medidata, Rave, Oracle OC/RDC, Oracle Inform, and/or ...

Sr. Clinical Programmer Syneos Health is a leading fully-integrated life sciences services ... Utilizes primary development tools including Medidata, Rave, Oracle OC/RDC, Oracle Inform, and/or ...

Veeva CDMS, Medidata RAVE, etc.) * Experience with Veeva EDC and Veeva CDB preferred * Proficient ... clinical systems and data administration * Must be organized, an effective written and oral ...

Veeva CDMS, Medidata RAVE, etc.) * Experience with Veeva EDC and Veeva CDB preferred * Proficient ... clinical systems and data administration * Must be organized, an effective written and oral ...

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Clinical Programmer Medidata Rave information

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

As of Jul 6, 2026, the average hourly pay for 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 in the Clinical Programmer Medidata Rave position, and why are they important?

To succeed as a Clinical Programmer Medidata Rave, you need a strong background in clinical data management, programming (such as SAS or SQL), and knowledge of clinical trial processes, often supported by a degree in life sciences, computer science, or a related field. Expertise in using Medidata Rave EDC, along with familiarity with CDISC standards and relevant certifications, is highly valued. Attention to detail, problem-solving ability, and effective communication are standout soft skills for this role. These competencies ensure accurate data capture, smooth collaboration with study teams, and the integrity of clinical trial results.

What are some common challenges faced by Clinical Programmers specializing in Medidata Rave, and how can they be addressed?

Clinical Programmers working with Medidata Rave often face challenges such as managing complex protocol requirements, ensuring data quality across large datasets, and adapting to evolving regulatory standards. Addressing these challenges usually involves staying current with system updates, maintaining clear documentation, and collaborating closely with data managers, biostatisticians, and clinical teams to resolve discrepancies efficiently. Effective troubleshooting skills and ongoing training on the Medidata Rave platform can also help streamline workflow. Being proactive in communicating potential issues and actively contributing to process improvements can set you apart and help ensure the success of clinical studies.

What is a Clinical Programmer Medidata Rave job?

A Clinical Programmer specializing in Medidata Rave is responsible for designing, developing, and maintaining electronic data capture (EDC) systems for clinical trials. They configure study databases, create edit checks, and ensure data integrity within the Medidata Rave platform. Additionally, they collaborate with clinical data managers and biostatisticians to streamline data collection and validation processes. Their role is crucial in optimizing clinical trial workflows and ensuring compliance with regulatory standards.

More about Clinical Programmer Medidata Rave jobs
What cities are hiring for Clinical Programmer Medidata Rave jobs? Cities with the most Clinical Programmer Medidata Rave job openings:
What are the most commonly searched types of Clinical Programmer Medidata Rave jobs? The most popular types of Clinical Programmer Medidata Rave jobs are:
Infographic showing various Clinical Programmer Medidata Rave job openings in the United States as of June 2026, with employment types broken down into 5% Locum Tenens, 90% As Needed, and 5% Full Time. Highlights an 90% Physical, 1% Hybrid, and 9% 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

Posted 17 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.