A Clinical Research Associate (CRA) is a healthcare and research professional responsible for monitoring and managing clinical trials to ensure they are conducted according to study protocols, regulatory guidelines, and ethical standards.

Key Responsibilities:

* Monitor clinical trial sites and ensure compliance with protocols, Good Clinical Practice (GCP), and regulatory requirements.

* Review study documents, source data, and case report forms (CRFs).

* Conduct site initiation, monitoring, and close-out visits.

* Verify the accuracy and completeness of clinical data collected during the study.

* Ensure patient safety and proper reporting of adverse events.

* Coordinate with investigators, study coordinators, sponsors, and other stakeholders.

* Maintain trial documentation and prepare monitoring reports.

* Support audit and inspection readiness throughout the study.

Required Skills:

* Knowledge of Clinical Research, ICH-GCP guidelines, and regulatory requirements.

* Solid attention to detail and problem-solving skills.

* Excellent communication and interpersonal abilities.

* Good documentation and reporting skills.

* Ability to manage multiple tasks and travel to clinical sites when required.

📌 Clinical Research Associate (Telangana)
🏢 Proxima Skills Training Consulting Services
📍 Telangana