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Mid Level Clinical Programmer Medidata Rave Jobs

Cytel

Senior EDC Programmer (Medidata)

Cambridge, MA · On-site +1

As a Senior EDC Programmer (Medidata) you bring deep expertise in designing, developing, and maintaining clinical databases using Medidata Rave. This role focuses on translating clinical protocol ...

Cytel

Senior EDC Programmer (Medidata)

Cambridge, MA · On-site +1

As a Senior EDC Programmer you bring deep expertise in designing, developing, and maintaining clinical databases using Medidata Rave. This role focuses on translating clinical protocol requirements ...

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 ...

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 ...

SystImmune Inc.

EDC Programmer

Redmond, WA · On-site

... a clinical trial environment. * Expert-level proficiency with Medidata Rave, including Rave ... While most offers typically fall within the low to mid-point of the range, we may extend an offer ...

Systimmune

EDC Programmer

Redmond, WA · On-site

$100K - $150K/yr

... a clinical trial environment. * Expert-level proficiency with Medidata Rave, including Rave ... While most offers typically fall within the low to mid-point of the range, we may extend an offer ...

SystImmune, Inc

EDC Programmer

Redmond, WA · On-site

$100K - $150K/yr

... a clinical trial environment. * Expert-level proficiency with Medidata Rave, including Rave ... While most offers typically fall within the low to mid-point of the range, we may extend an offer ...

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 ...

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 ...

Immunome, Inc.

SeniorEDC Programmer

Bothell, WA · On-site

Position Overview The Senior EDC (Electronic Data Capture) Programmer (Sr. EDCP) is responsible for ... Medidata Rave preferred). * Solid understanding of clinical trial processes and data flow.

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As of Jun 27, 2026, the average hourly pay for mid level 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.
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Mid Level Clinical Programmer Medidata Rave jobs near you
Senior EDC Programmer (Medidata)

Senior EDC Programmer (Medidata)

Cytel

Cambridge, MA • On-site, Remote

Full-time

Posted 22 days ago

Job description


As a Senior EDC Programmer (Medidata) you bring deep expertise in designing, developing, and maintaining clinical databases using Medidata Rave. This role focuses on translating clinical protocol requirements into efficient, high-quality EDC solutions, including CRF design, edit checks, derivations, and integrations, while ensuring compliance with regulatory standards and industry best practices. With strong collaboration across data management, biostatistics, and clinical teams, the Senior EDC Developer plays a critical role in delivering accurate, reliable, and scalable database builds that support successful clinical trial execution.
Responsibilities
Key Responsibilities:
  • Serve as Subject Matter Expert (SME) for Medidata Rave and related Medidata applications (Core Configuration, eLearning Assignment, Reporter Assignment, Local Lab, Safety Gateway, TSDV, Batch Uploader, Imaging), advising and mentoring cross-functional teams across Data Management, Statistical Programming, Clinical Operations, and external partners.
  • Lead and oversee EDC database builds in Medidata Rave, including CRF design, edit checks, derivations, code lists, user roles, and integrations, ensuring alignment with protocol requirements and industry best practices.
  • Maintain and govern core EDC configuration standards, reusable libraries, and study design conventions to ensure consistency, quality, and efficiency across all studies.
  • Maintain and manage Cloud Admin EDC roles, ensuring appropriate access control, compliance, and standardized role usage across studies.
  • Proactively communicate updates, changes, and potential impacts related to core configuration and Cloud Admin roles to internal teams and stakeholders.
  • Review, assess, and interpret Medidata release notes, platform updates, revised eLearnings, and Rave reports; evaluate impact on ongoing and upcoming studies.
  • Translate Medidata system updates and enhancements into clear, actionable guidance and training for study teams.
  • Act as a primary liaison between key stakeholders, ensuring alignment on EDC design, build standards, timelines, and issue resolution.
  • Act as a liaison between Data Management and Statistical Programming to ensure data collection strategies support downstream analysis, reporting, and regulatory submission requirements.
  • Collaborate with business owners of other Medidata applications (e.g., Coder, Safety Gateway, CTMS,, eCOA, Imaging) to support integrated data workflows and a cohesive clinical data ecosystem.
  • Experience with integrating non Medidata systems such as RBQM, CTMS, IRT, and data cleaning tools with Medidata.
  • Provide ongoing consultation on EDC best practices, system capabilities, and process improvements to support high-quality, compliant clinical trial execution.

Qualifications
  • At least 8 years progressive Clinical Research Experience
  • Medidata Rave Certified Study Builder
  • 6 years' experience as a database programmer
  • Bachelor's degree Required

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