Senior Consultant - Clinical Data Programming
Core
Senior Consultant acting as a trusted advisor to configure Veeva Vault CDMS and DQS for clinical trials, optimizing EDC usage and developing custom SQL listings.
Role type
Senior IC clinical data programming consultant
Builds
Configured clinical trial databases, custom SQL listings, and data ingestion pipelines for life sciences customers
Domain
Life sciences / Clinical trials / SaaS
Deliverable
production ML models | product features | dashboards & analysis | client delivery
Required skills
EDC clinical software programming, SQL-based language development, clinical protocol interpretation, database design, data collection and review, customer-facing consulting, project specification creation
Preferred skills
SAS, R, JSON, Python, REST-based APIs, data management standards (GCDMP, CDISC, SDTMIG, CDASH, ADaM), system integrator experience, Veeva applications knowledge
Technologies
Veeva Vault CDMS, Veeva Data Quality System (DQS), SQL, SAS, R, JSON, Python
Responsibilities
Configure forms, rules, and study items in Veeva Vault CDMS; develop custom SQL-based listings; configure data ingestions into Veeva DQS; consult with customers on clinical protocol requirements; drive database development with sponsor/CRO teams; conduct user acceptance testing; support study integrations and go-live activities
Seniority
Senior, hands-on IC
