Scientist Drug Safety (Temporary)
Core
Support safety reporting in clinical trials across multiple therapeutic areas for investigational product development in early and late-stage programs.
Role type
Clinical Safety Scientist (CSS)
Builds
Safety reports and case data for clinical trials
Domain
Pharmaceutical development / Drug safety
Deliverable
client delivery
Required skills
Clinical safety reporting, GCP and ICH regulations, Clinical trial data management, Safety query generation, Cross-functional collaboration, Medical concept understanding, Drug development knowledge, Time management, Problem escalation, Database management
Preferred skills
Safety reporting
Technologies
Safety databases
Responsibilities
Intake reportable safety event information from investigator sites, Review and manage individual case safety reports, Ensure clinical completeness and accuracy of case information, Generate safety queries to trial investigator sites, Prioritize daily work for safety database submission, Complete protocol-specific activities, Escalate protocol or event issues to stakeholders
Seniority
Entry-level to Junior, hands-on IC