Job Summary
A company is looking for a Clinical Trial Professional.
Key Responsibilities
- Manage day-to-day operations of assigned clinical trials to ensure deliverables are met
- Coordinate study timelines and communicate with internal team members regarding deliverables
- Provide oversight and direction to study team members and manage trial feasibility and site selection
Required Qualifications
- 5-10+ years of trial coordination experience in a clinical research environment
- Experience in Oncology or Neurology is required
- Relevant experience in global settings managing CROs and multiple study vendors
- Bachelor's degree in a clinical or science-based subject
- Solid understanding of drug development and FDA/ICH GCP guidelines
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