Conducting site initiation, monitoring, and close-out visits.
Ensuring compliance with GCP, ICH guidelines, and regulatory requirements.
Reviewing and verifying clinical trial data.
Monitoring site performance and patient safety.
Managing and resolving site-related issues.
Maintaining accurate and complete study documentation.
Communicating with investigators, site staff, and sponsors.
Source data verification.
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Employement Category:
Employement Type: Full time Industry: Pharma / Biotech Role Category: Pharmacist / Medical Representative Functional Area: Not Specified Role/Responsibilies: Clinical Research Associate Job in CLIN