Sr EDC Developer

Required Skills & Experience

• Hands-on experience developing and configuring EDC systems within a clinical research environment.
• Experience designing and building eCRFs for clinical trials or research studies.
• Experience implementing validation rules, edit checks, required-field logic, and data consistency checks.
• Strong understanding of clinical research workflows and clinical trial data collection.
• Experience supporting clinical research within a pharmaceutical, biotechnology, CRO, academic medical center, or similar clinical research organization.
• Ability to translate clinical study requirements into scalable, user-friendly EDC solutions.
• Strong organizational, problem-solving, and communication skills. Ability to work independently and collaborate with both technical and clinical stakeholders.

Nice to Have Skills & Experience

• Hands-on experience with Veeva EDC / Veeva Vault Clinical Suite.
• Experience with Medidata Rave or a comparable clinical EDC platform.
• Experience working with Global Library / Global Librarian functionality, reusable forms, or standardized clinical study libraries.
• Experience within an oncology or cancer research environment.
• Experience developing EDC standards, templates, or processes for a growing clinical research program. Experience working within a pharmaceutical company, biotechnology company, CRO, or academic research environment.

Job Description

We are seeking an experienced Senior EDC Developer to support the development and expansion of a clinical research technology function focused on electronic data capture for clinical trials. This individual will play a key role in designing, building, and configuring electronic case report forms (eCRFs) used across clinical research studies. The Senior EDC Developer will work closely with clinical research stakeholders to translate study requirements into effective EDC solutions while helping establish scalable standards, reusable templates, and development best practices. This is an excellent opportunity for an experienced clinical EDC professional who enjoys being hands-on while also helping shape processes and standards for a growing program.

Key Responsibilites:

• Design, build, and configure electronic case report forms (eCRFs) for clinical research studies.
• Develop and configure forms within Veeva EDC to capture clinical trial data, including demographics, laboratory results, vital signs, adverse events, visit information, and other study-specific data.
• Create and maintain field requirements, validation rules, edit checks, and cross-form consistency checks to support high-quality clinical data.
• Translate study protocols and business requirements into effective EDC configurations.
• Develop standardized and reusable forms, templates, and libraries that can be leveraged across multiple clinical studies.
• Help establish development standards, best practices, and processes for a growing EDC development function.
• Partner with clinical research, data management, and other stakeholders throughout the study development lifecycle.
• Serve as a senior technical resource and provide expertise around EDC design and configuration.