Clinical Research Associate

Saurav Shrikant Tambde

Madurai, Tamil Nadu

Objectives Of This Role

Ensuring compliance with protocols, standard operating procedures, and Good Clinical Practice (GCP) guidelines.

Conducting regular site visits to monitor trial activities and data collection.

Reviewing and analysing clinical trial data for accuracy and completeness.

Developing and maintaining study timelines and budgets.

Providing training to study staff on study protocols and GCP guidelines.

Your Tasks

Reviewing and approving study-related documents, such as informed consent forms.

Conducting source data verification and ensuring data quality.

Managing trial supplies and drug accountability.

Serving as a liaison between study sites, sponsors and regulatory agencies.

For More details Contact:-8860569880

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