On-site Central Study Coordinator/Research Assistant - Santa Fe, Argentina
ProPharma(3 months ago)
About this role
The Central Study Coordinator/Research Assistant is an early-career clinical research role supporting ProPharma’s study operations within its consultancy serving biotech, medical device, and pharmaceutical clients. The position is based onsite in Santa Fe, Argentina and contributes to the execution and oversight of assigned clinical projects. Candidates work as part of study teams to support compliant clinical trial processes.
Required Skills
- Site Communications
- Recruitment
- Reconsenting
- Medical Records
- Data Entry
- Database Monitoring
- IRB Compliance
- GCP
- SOPs
- Protocol Activities
+2 more
Qualifications
- Bachelor's Degree
About ProPharma
propharmagroup.comProPharma helps navigate the complexities of drug development and ensure patient health and safety throughout the product lifecycle.
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