Senior Consultant - Clinical Data Programming
Core
Senior Consultant acting as a trusted advisor to configure and support clinical trial data management systems (Vault CDMS/DQS) for life sciences customers.
Role type
Senior IC clinical data programming consultant
Builds
Configured clinical trial databases, data cleaning listings, and study integrations for pharma/biotech clients
Domain
Life Sciences / Clinical Data Management
Deliverable
production ML models | product features | dashboards & analysis | client delivery
Required skills
EDC clinical software expertise, clinical trial data management, SQL/Python/R/SAS programming, customer-facing consulting, database design, query resolution, statistical reporting
Preferred skills
GCDMP/CDISC/SDTMIG standards, REST API integration, system integrator experience, Veeva platform familiarity
Technologies
Vault CDMS, Veeva DQS, SQL, Python, R, SAS, JSON
Responsibilities
Configure forms, rules, and study items in Vault CDMS; build custom SQL-based listings for data cleaning; coordinate with clinical data providers (labs, ECG, eCOA); lead database development and user acceptance testing; interpret clinical protocols and project specifications; support study integrations and go-live activities; flag risks and contingency plans to project management.
Seniority
Senior, hands-on IC
