On-site Central Study Coordinator/Research Assistant - Buenos Aires, Argentina
ProPharma(3 months ago)
About this role
The Central Study Coordinator/Research Assistant at ProPharma coordinates and supports remote site activities for assigned clinical research projects. The role acts as a point of contact for site communications, supports participant screening and consenting, and helps maintain regulatory-compliant study documentation throughout the study lifecycle.
Required Skills
- Clinical Research
- Patient Recruitment
- Informed Consent
- Data Entry
- Clinical Databases
- Regulatory Compliance
- ICH-GCP
- SOPs
- Communication
- Critical Thinking
+4 more
Qualifications
- Bachelor's Degree
- 2 Years Study Coordinator Experience
- 1 Year Research Experience
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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