Associate Director, Clinical Sciences, Oncology
About this role
The Role
This role will support Oncology Therapeutic programs, specifically supporting the Clinical Study Lead in the development, execution and evaluation of Phase 1-3 clinical studies. The principal responsibility for this role is to ensure the comprehensive data quality of clinical studies to support both internal governance decisions and regulatory submissions.
Here’s What You’ll Do
Broadly stated, in conjunction with the Clinical Study Lead and the broader Clinical Trial Team, oversee end-to-end delivery of clinical trial protocols including study design, initiation, medical safety data monitoring, data dissemination and closeout activities.
Specifically:
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