Clinical Trial Assistant

0 - 2 years

2 - 4 Lacs

Posted:15 hours ago| Platform: Naukri logo

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Job Type

Full Time

Job Description

Roles and Responsibility
  • Assist in the planning, execution, and monitoring of clinical trials to ensure compliance with regulatory requirements.
  • Collaborate with cross-functional teams to develop and implement study protocols and case report forms.
  • Conduct site feasibility assessments and coordinate with investigators to ensure timely and accurate data submission.
  • Develop and maintain study databases and track systems for timely updates on study progress.
  • Coordinate with internal stakeholders to resolve issues related to study start-up, patient enrollment, and protocol deviations.
  • Ensure adherence to Good Clinical Practice (GCP) guidelines and maintain high standards of quality control.

Disclaimer: This job description has been sourced from a public domain and may have been modified by Naukri.com to improve clarity for our users. We encourage job seekers to verify all details directly with the employer via their official channels before applying.

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