EDC Clinical Programmer

Redbock - an NES Fircroft company; United States; On-site; USD 140,000 - 170,000; Full time

Job summary

The EDC Programmer will serve as the internal subject matter expert for Veeva EDC, supporting the transition of clinical data management and EDC programming activities from CRO partners to an in-house model. This role will be responsible for study builds, edit check programming, custom function development, RTSM integrations, system administration, testing, and ongoing support of clinical studies.

Working closely with Clinical Data Management, Clinical Operations, Biostatistics, and external

Qualifications

• Bachelor's degree in a related field or higher.
• 5+ years of clinical trial EDC programming experience.
• Hands-on Veeva EDC study builds, configuration, and administration.
• Strong skills in edit checks, derivations, and study logic.
• Experience designing, testing, and supporting RTSM-EDC integrations.
• Understanding of GCP and data management processes.
• Experience supporting UAT, releases, and database lock activities.
• Ability to transition CRO functions to an in-house team.
• Excellent problem-solving, communication, and collaboration.

Responsibilities

• Build and validate EDC studies and edit checks.
• Configure custom functions and study logic.
• Support RTSM-EDC integrations and data flows.
• Administer EDC systems, testing, and deployments.
• Lead the transition of CRO functions to internal team.

Skills

EDC programming

Veeva EDC

Study builds

Edit checks & derivations

RTSM integrations

System administration

UAT support

Cross-functional collaboration

Communication

Education

Bachelor's degree in Computer Science, Information Systems, Life Sciences, or related field

Tools

Veeva EDC

RTSM Integrations

System administration tools

Job description

The EDC Programmer will serve as the internal subject matter expert for Veeva EDC, supporting the transition of clinical data management and EDC programming activities from CRO partners to an in-house model. This role will be responsible for study builds, edit check programming, custom function development, RTSM integrations, system administration, testing, and ongoing support of clinical studies. Working closely with Clinical Data Management, Clinical Operations, Biostatistics, and external vendors, the individual will ensure high-quality, compliant, and efficient data collection processes while helping establish scalable standards and best practices in a growing, small-company environment.

Required Qualifications

• Bachelor's degree in Computer Science, Information Systems, Life Sciences, or related field.
• 5+ years of clinical trial EDC programming experience within biotech, pharmaceutical, or CRO environments.
• Hands-on experience with Veeva EDC study builds, configuration, and system administration.
• Strong experience programming and validating edit checks, custom functions, derivations, and study logic.
• Experience designing, testing, and supporting RTSM-EDC integrations.
• Understanding of clinical trial conduct, data management processes, and GCP requirements.
• Experience supporting UAT, database releases, and database lock activities.
• Ability to independently manage EDC activities and drive the transition of functions from CROs to an internal team.
• Excellent problem-solving, communication, and cross-functional collaboration skills.

Prior experience working in a small or emerging biotech company, with the flexibility to build processes and operate in a hands-on, fast-paced environment.