Hiring Clinical Research Associate_Udaipur

Role & responsibilities

• Study Site Management & Regulatory Compliance
• Conducting initiation visits to ensure sites are prepared for the trial.
• Regularly visiting study sites to ensure compliance with the protocol, Good Clinical Practice (GCP), and regulatory requirements.
• Ensuring that the study is conducted in accordance with the approved protocol and amendments. Verifying that informed consent is obtained from all study participants.
• Data Quality and Integrity
• Risk Management
• Implementing corrective and preventive actions (CAPA) to resolve issues and prevent recurrence.
• Documentation and Reporting - Ensuring all trial-related documentation is complete, accurate, and up-to-date. Preparing monitoring reports, site visit reports, and other required documentation.
• Patient Safety and Rights - Monitoring and reporting adverse events and serious adverse events (SAEs) in accordance with regulatory requirements. Ensuring the safety and well-being of study participants throughout the trial.

Preferred candidate profile

• Masters in Science / PHD / Relevant qualification in Clinical Research
• Mandatory to have: Should have lead a team of CRC in past for minimum 3 - 4 years