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Clinical Programmer Medidata Rave Jobs (NOW HIRING)

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 ...

Fortrea

$80K - $95K/yr

Lead the development and implementation of Clinical solutions to global technical services issues ... Complete assigned work utilizing Medidata Rave or Oracle Inform or other proprietary software ...

Fortrea

Senior Programmer Analyst

Durham, NC · Remote

$80K - $95K/yr

Lead the development and implementation of Clinical solutions to global technical services issues ... Complete assigned work utilizing Medidata Rave or Oracle Inform or other proprietary software ...

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 ...

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 Aug 16, 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 as a clinical programmer Medidata Rave?

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?

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 August 2026, with employment types broken down into 3% As Needed, 72% Full Time, 17% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $134,731 per year, or $64.8 per hour.

Medidata Rave | Clinical Programmer (Remote, Full Time)-LC0002

TechData Service Company LLC

King Of Prussia, PA • Remote

$90K - $150K/yr

Full-time

Medical, Dental, Retirement, PTO

Posted 16 days ago

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Job description

Qualifications:

•5+ years of EDC database build experience for clinical trial.

•Experience with Medidata Rave with Medidata certification; Minimum two to three years current database programming experience designing studies and data validation programming in Medidata Rave.

•Is able to write the code at CF from scratch.

•Familiarity with clinical data regulations (GCP, ICH).

•Familiarity with Operational Qualification/Performance Qualification and UAT execution and documentation.

•BS or MS degree in related discipline.

Responsibilities:

•Build and design clinical study trials in Medidata RAVE system.

•Design/create and test clinical databases including forms, folders, matrices, data

dictionaries/code lists, unit dictionaries, edit checks/rules, derivations, custom functions, standard and custom reports.

•Provide programming expertise to support data capture, review, and monitoring for clinical trials.

•Program reports, edit checks, and custom functions based on study protocol requirements.

•Assist with EDC integration with other systems, including but not limited to IRT system, CTMS system and etc.

•Manage external vendor data import and validation.

•Provide technical support as needed for Medidata RAVE and Merative Zelta EDC systems.

•Participate in EDC design requirements development in collaboration with Study Lead Data Manager and the wider study team.

•Support development of and updates of global library objects as appropriate according to best practices and new standards.

•Perform peer review for the studies built by other programmers.

•Maintain all required Clinical Systems study documentation.

•Provide EDC technical support to facilitate study timelines and deliverables.

•Manage timely-quality deliverables for the study teams for assigned protocol/study(s).

TechData is proud to be an equal opportunity workplace and is an affirmative action employer. We are committed to equal employment opportunity regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity or Veteran status.

Company Description

https://quantive.bio/