Senior Programmer, EDC Systems (Clinical Data)

Location: Waltham, Massachusetts, USA; onsite/hybrid attendance with a minimum of 3 days per week in the designated office. Relocation and mobility assistance are not provided.

Salary: $143,000–$169,000 annual base salary, with potential incentive compensation and equity.

Company

hirify.global is a global biotherapeutics company developing therapies, vaccines, and other medicines for serious and rare diseases.

What you will do

• Design, develop, and maintain clinical study databases, including CRFs, edit checks, reports, custom programs, and system interfaces.
• Define and enhance data quality methods, acceptance criteria, and validation rules for eCRFs and external data sources.
• Govern validation check libraries, standardized reports, listings, and recurring operational and data-quality reporting.
• Review and validate clinical data deliverables with Data Management, Statistics, Standards, and vendors to support submission readiness.
• Support data structures, storage, integrations, and external sources such as IxRS, eDiaries, laboratory, and ECG data.
• Contribute to scalable data platforms, automation strategies, and AI-enabled capabilities for clinical data processing and analytics.

Requirements

• 5+ years of relevant experience designing clinical databases in EDC systems within a pharmaceutical or CRO environment.
• Proficiency with EDC systems such as Medidata Rave or Veeva Vault, including eCRF design and clinical data collection frameworks.
• Practical knowledge of CDISC standards, especially CDASH and SDTM, including data mapping, validation, and submission-readiness activities.
• Strong understanding of clinical data processes, data flows, integrations, quality oversight, validation, and vendor deliverable review.
• BSc in Computer Science, Mathematics, Statistics, or a related field, plus relevant experience.
• Fluent written and spoken English and availability for onsite/hybrid work in the United States are required.

Nice to have

• Medidata Rave Study Builder Certification.
• Experience with post-production data migration activities.
• Experience with C#.
• Familiarity with SAS, Python, or R.

Culture & Benefits

• Full-time employment with compensation that may include incentive pay and equity.
• Benefits supporting employee well-being.
• Inclusive workplace focused on belonging, curiosity, empathy, and collaboration.
• Work across in-house, hybrid, and vendor-supported clinical studies within a global organization.