Central Study Coordinator - PARTTIME (0.25 FTE)
ProPharma(1 month ago)
About this role
The Central Study Coordinator at ProPharma supports remote clinical study operations for biotech, medical device, and pharmaceutical clients. This part-time (0.25 FTE / 10 hours/week) remote role sits within the company’s clinical research consulting services and contributes to the coordination and oversight of study activities to help advance product development. The role interfaces with study teams and site personnel to maintain regulatory compliance and study continuity.
Required Skills
- Site Communication
- Document Submission
- Recruitment
- Medical Records
- Protocol Activities
- Data Entry
- Database Monitoring
- IRB Compliance
- Regulatory Knowledge
- GCP
+6 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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