Posted:5 days ago| Platform: Shine logo

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Work Mode

On-site

Job Type

Full Time

Job Description

 

  • Assist in preparing essential trial documents (Investigator Site File, Trial Master File, etc.).

  • Support site selection, initiation, monitoring, and close-out activities.

  • Ensure accuracy and completeness of study documents.

  • Support senior CRAs during routine monitoring visits.

  • Verify source documents, patient eligibility, and informed consent forms.

  • Ensure adherence to study protocols and GCP norms.

  • Assist in data collection, query resolution, and CRF/EDC data entry checks.

  • Ensure timely reporting of deviations and adverse events.

  • Ensure that all trial activities follow SOPs, regulatory guidelines, ICH-GCP, and ethical standards.

  • Maintain confidentiality and integrity of clinical trial data.

  • Coordinate between investigators, study coordinators, and project teams.

  • Attend training sessions, investigator meetings, and team discussions.

 

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