Clinical Research Associate (Spanish Speaking)
ProPharma(1 month ago)
About this role
The Contract Clinical Research Associate (CCRA) at ProPharma is responsible for executing and managing clinical study activities and site management deliverables across assigned protocols. The role partners with sponsors, investigators, and internal project teams to support study conduct, data integrity, and regulatory compliance across the product lifecycle.
Required Skills
- Site Management
- Monitoring
- GCP
- Protocol Compliance
- Data Management
- EDC
- Communication
- Regulatory Compliance
- Source Data Verification
- eTMF
+1 more
Qualifications
- Bachelor's Degree
- Associate Degree
- High School Diploma
- Clinical Research Certification
- Authorization To Work In The United States Without Sponsorship
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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