
(MI-778) | Start-up Specialist
- Buenos Aires
- Permanente
- Tiempo completo
Minimum 2 years of experience in clinical development or regulatory process. Working knowledge of ICH, FDA, IRB/IEC, and other applicable regulations/guidelines; familiarity with investigator start-up documents and contract/budgets negotiation process; previous interaction with operational project teams and investigative sites
- Demonstrated understanding of research protocol requirements and proven ability to communicate with/educate others about them**Labcorp is proud to be an Equal Opportunity Employer**:
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