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Volunteer Clinical Programmer Medidata Rave Jobs

CTI

Clinical Programmer

Covington, KY · On-site +1

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 ...

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 ...

CTI

Clinical Programmer

Covington, KY · On-site +1

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 ...

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 ...

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SystImmune Inc.

EDC Programmer

Redmond, WA · On-site

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 ...

Syneoshealth

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 ...

Syneoshealth

Sr. Clinical Programmer

New York, NY · On-site

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 ...

Syneoshealth

Sr. Clinical Programmer

Concord, NC

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 ...

Celerion

EDC Developer / Programmer

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 ...

Celerion

EDC Developer / Programmer

OR · Remote

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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All JobsVolunteer Clinical Programmer Medidata Rave Jobs

Volunteer Clinical Programmer Medidata Rave information

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

As of Jul 6, 2026, the average hourly pay for volunteer 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 is the difference between Volunteer Clinical Programmer Medidata Rave vs Clinical Data Coordinator?

AspectVolunteer Clinical Programmer Medidata RaveClinical Data Coordinator
CredentialsBasic programming knowledge, familiarity with Medidata RaveDegree in health sciences or related field, data management experience
Work EnvironmentClinical trial data management, using Medidata Rave softwareData collection, entry, and quality control in clinical settings
Employer & IndustryPharmaceutical companies, CROs, biotech firmsHospitals, research institutions, clinical trial sites

The Volunteer Clinical Programmer Medidata Rave primarily focuses on configuring and managing clinical trial data within the Medidata Rave platform, often on a volunteer basis. In contrast, a Clinical Data Coordinator handles broader data management tasks, including data entry, validation, and quality assurance. While both roles require knowledge of clinical data processes, the Programmer role emphasizes technical software skills, whereas the Coordinator role involves more administrative and oversight responsibilities.

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

To thrive as a Volunteer Clinical Programmer Medidata Rave, you need a solid understanding of clinical data management, programming principles (such as SQL or SAS), and familiarity with clinical trial processes, often supported by a degree in life sciences, computer science, or a related field. Proficiency with Medidata Rave EDC systems, CRF design, and data validation tools, as well as knowledge of CDISC standards, are typically required. Attention to detail, problem-solving ability, and strong communication skills help ensure data integrity and effective collaboration with study teams. These competencies are crucial for delivering accurate, compliant clinical data that support successful clinical trial outcomes.

What is a Volunteer Clinical Programmer Medidata Rave?

A Volunteer Clinical Programmer Medidata Rave is an individual who assists with programming tasks related to clinical trials using the Medidata Rave electronic data capture (EDC) system, typically on a volunteer or unpaid basis. Their main responsibilities include designing and building electronic case report forms (eCRFs), programming edit checks, and ensuring data integrity within the Rave platform. They work closely with clinical data managers and study teams to support the accurate and efficient collection of clinical trial data. This role is ideal for those seeking to gain experience in clinical data management and clinical programming, especially with the widely used Medidata Rave system.

What are some common challenges faced by a Volunteer Clinical Programmer working with Medidata Rave, and how can they be addressed?

Volunteer Clinical Programmers using Medidata Rave often face challenges such as adapting to strict data standards, managing complex study protocols, and ensuring data quality within tight timelines. Since volunteers may have limited prior exposure to the organization's specific workflows, familiarizing yourself with Medidata Rave's interface and standard operating procedures is crucial. Collaborating closely with clinical data managers and IT teams can help resolve data discrepancies quickly and ensure compliance with regulatory requirements. Proactively seeking training resources and participating in team meetings will help you stay aligned with project goals and improve your technical proficiency.
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Volunteer Clinical Programmer Medidata Rave jobs near you
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.

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