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Clinical Programmer Medidata Rave Jobs (NOW HIRING)

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

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 ...

Immunome, Inc.

SeniorEDC Programmer

Bothell, WA

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.

MapLight Therapeutics

Clinical Data Manager

Burlington, MA · On-site

$145K - $160K/yr

MapLight Therapeutics is a clinical stage biotech company that focuses on drug discovery for ... Oversee Medidata Rave electronic data capture (EDC) system setup, configuration, user management ...

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

As of Jun 15, 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.

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Clinical Programmer Medidata Rave jobs near you
Infographic showing various Clinical Programmer Medidata Rave job openings in the United States as of June 2026, with employment types broken down into 86% Full Time, and 14% Contract. Highlights an 71% In-person, and 29% Remote job distribution, with an average salary of $134,731 per year, or $64.8 per hour.
Senior EDC Programmer (Medidata)

Senior EDC Programmer (Medidata)

Cytel

Cambridge, MA • On-site, Remote

Full-time

Posted 11 days ago

Job description

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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