Associate Director, Clinical Trial Safety Scientist
Core
Review large volumes of medical safety data from clinical trials to ensure patient data completeness and medical accuracy for study physicians and scientists.
Role type
Senior individual contributor clinical safety scientist with program leadership responsibilities
Builds
Consolidated safety data packages and standardized review processes for late-stage and early-phase clinical trials
Domain
Pharmaceutical clinical trials / medical safety data
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work
Required skills
Clinical data review, medical safety evaluation, program/molecule/indication level oversight, cross-functional collaboration, team resourcing and training, risk escalation, talent retention
Preferred skills
Experience with study start-up, maintenance, and closure activities, data querying and coding consistency checks, performance management metrics
Technologies
Clinical trial management systems, safety data review tools
Responsibilities
Oversee implementation and ongoing review of critical clinical/safety data, ensure seamless data review, support team handling of data querying, collect feedback and share lessons learned, report and escalate risks to the Director, assist with recruiting and retaining talent
Seniority
Associate Director, hands-on IC with management duties