Senior Consultant - Clinical Data Programming
Core
Senior consultant advising life sciences customers on optimizing EDC usage and configuring Veeva Vault CDMS/DQS for clinical trials.
Role type
Senior IC clinical data programming consultant
Builds
Configured clinical trial data management systems (Veeva Vault CDMS/DQS) and custom SQL listings
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, query resolution, statistical reporting, customer-facing consulting, project management
Preferred skills
SAS, R, JSON, Python, REST-based APIs, data management standards (GCDMP, CDISC, SDTMIG, CDASH, ADaM), system integrator experience, Veeva applications experience
Technologies
Veeva Vault CDMS, Veeva Data Quality System (DQS), SQL, SAS, R, JSON, Python
Responsibilities
Act as trusted advisor to ensure study trial design meets customer goals; consult on clinical protocol requirements and project specifications; drive database development with sponsor/CRO teams; configure forms, rules, and study items; develop custom SQL-based listings; conduct user acceptance testing; support requirements gathering for integrations; communicate risks and contingency plans; contribute to product best practices.
Seniority
Senior, hands-on IC
