Cra / Senior Cra Noida (India)

Hiring: CRA / Senior CRA

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? Location: Noida

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We are looking for experienced Clinical Research Associates to join a growing Clinical Affairs team.

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Key Responsibilities

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• Clinical trial handling and site management

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• CRO coordination and monitoring activities

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• Ethics Committee submissions and regulatory documentation

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• Site initiation, monitoring, and close -out activities

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• Training site staff on protocols and GCP requirements

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• Subject safety and compliance management

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• Investigational Product accountability and reconciliation

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• Preparation of monitoring reports and study documentation

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• Ensuring compliance with ICH -GCP guidelines and SOPs

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Requirements

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• 3–5 years of Clinical Research experience

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• Solid experience in Clinical Trial Handling

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• Hands -on exposure to CRO Management

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• Experience in Ethics Committee submissions

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• Valuable understanding of ICH -GCP and regulatory requirements

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Interested candidates can share their updated resume.

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