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, Valuable 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.
Valuable 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