Clinical Research Associate ( CRA )

2 - 4 years

2 Lacs

Posted:3 hours ago| Platform: Naukri logo

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Job Type

Full Time

Job Description

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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