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60 Edc Full Time Jobs Hiring Near You

Celerion

Veeva Clinical Database Programmer

This is a full-time, remote opportunity, but you may travel for training and key meetings. As a Veeva Clinical Database Programmer , you will build and administer EDC trials for client-contracted ...

Celerion

Veeva Clinical Database Programmer

This is a full-time, remote opportunity, but you may travel for training and key meetings. As a Veeva Clinical Database Programmer , you will build and administer EDC trials for client-contracted ...

Celerion

Veeva Clinical Database Programmer

OR · Remote

This is a full-time, remote opportunity, but you may travel for training and key meetings. As a Veeva Clinical Database Programmer , you will build and administer EDC trials for client-contracted ...

Fortrea

Senior Programmer Analyst- Remote, US

$80K - $95K/yr

Perform any postproduction changes to the EDC database or enhancements to the SAS programs like SAS ... Regular, full-time or part-time employees working 20 or more hours per week are eligible for ...

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Infographic showing various Full Time job openings at Edc in the United States as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% Physical job distribution.

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 18 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/