As a Study Management Associate III, you will be part of a dynamic, centralized study management team responsible for the execution of global clinical trials. You will work as an independent, contributing member of a cross-functional and global partnership to plan, execute, and manage one or more Phase 0-4 clinical trials under the guidance of the Study Project Manager and SMA Manager.
Requirements
- Bachelor's Degree
- 4+ years of progressive Pharma-related/clinical research-related experience
- Competent in application of standard quality procedures (SOP, ICH/GCP, Global Regulations)
- Experienced user of systems such as EDC, IRT, CTMS, and eTMF
Benefits
- Equal Opportunity Employer
- Commitment to operating with integrity, driving innovation, transforming lives and serving our community
