Clinical Research Associate
5 days ago
The Clinical Research Associate will oversee clinical trial activities to ensure ethical conduct, regulatory compliance, and high-quality data generation.
Roles & Responsibilities:
- Assist in planning, initiation, execution, and closure of clinical trials.
- Conduct site monitoring visits (site selection, initiation, monitoring, close-out).
- Ensure adherence to study protocols, ICH-GCP, and regulatory requirements.
- Manage informed consent process and patient safety reporting.
- Coordinate with investigators, site staff, and CROs.
- Review Case Report Forms (CRFs) for accuracy and completeness.
- Track study timelines, budgets, and milestones.
- Support inspection readiness and audit activities.
- Maintain Trial Master File (TMF) and essential documents.
Interview Process: Assessment test, F2F interview.
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