EDC Programmer

Scorpion Therapeutics; United States; Remote; USD 110,000 - 160,000; Full time

Job summary

Scorpion Therapeutics seeks an EDC Programmer to design, develop, validate, and maintain electronic data capture systems for clinical trials in bladder cancer. You will build and validate high-quality EDC databases (Medidata Rave and Zelta), create edit checks, and support database lock, ensuring data integrity and regulatory compliance.

Collaborating with Data Management, Biostatistics, Clinical Operations, and external vendors, you’ll ensure adherence to CDISC standards and 21 CFR Part 11,

Qualifications

• Bachelor’s or Master’s in Computer Science, Life Sciences, or related field.
• 5+ years of EDC programming experience in pharma/biotech.
• Proficiency with Medidata Rave and Zelta.
• Understanding of clinical trial processes, data flow, and CDISC standards.

Responsibilities

• Build and validate high-quality, compliant EDC databases (Medidata Rave and Zelta).
• Develop edit checks and custom functions; support database lock.
• Ensure data integrity and regulatory compliance across trials.

Skills

EDC programming

Regulatory compliance

Cross-functional collaboration

CDISC knowledge

Education

Bachelor's or Master’s in Computer Science or Life Sciences

Tools

Medidata Rave

Zelta

Job description

Role

EDC Programmer responsible for designing, developing, validating, and maintaining electronic data capture systems to support clinical trials in bladder cancer.

Responsibilities

build and validate high-quality, compliant EDC databases (Medidata Rave and Zelta), develop edit checks and custom functions, support database lock, and ensure data integrity and regulatory compliance. Collaborates cross-functionally with Data Management, Biostatistics, Clinical Operations, and external vendors. Ensures adherence to CDISC standards, 21CFR Part11, and internal SOPs. Manages user access governance and audit trails to maintain inspection readiness.

Requirements

Bachelor's orMaster's in Computer Science, Life Sciences, or related field; 5+ years of EDC programming experience in pharma/biotech; proficiencywith Medidata Rave and Zelta platforms; understanding of clinical trial processes, data flow, and CDISC standards.

Preferred

experience supporting validation and UAT, CRO/vendor collaboration.

High-value

focuson clinical trials in bladder cancer, electronic data systems, GxP compliance, and cross-functional collaboration in a remote work environment.