Senior Scientist
Core
Plan, manage, and monitor in vivo nonclinical safety studies for oncology, inflammation, general medicine, and rare disease therapeutic areas.
Role type
Senior Scientist (Nonclinical Safety)
Builds
Nonclinical safety study protocols, reports, and data analysis for drug development programs.
Domain
Biotechnology / Nonclinical Safety / In Vivo Studies
Deliverable
client delivery
Required skills
in vivo nonclinical safety study management, GLP guidelines compliance, data analysis and interpretation, SOP development, cross-functional collaboration
Preferred skills
study director/monitor experience, CRO collaboration, program management principles, negotiation and influencing, people management
Technologies
Planisware, Gantt charts, graphing software
Responsibilities
Plan and monitor outsourced in vivo nonclinical safety studies; serve as primary contact for study protocols and reports; prepare scientific figures and presentations; write departmental guidelines and SOPs; facilitate meetings and report study status; manage complex issues involving multiple parties.
Seniority
Senior, hands-on IC with management responsibilities
