Clinical Research Associate (CRA)

Job Description

Responsibilities: Monitor clinical trials to ensure adherence to protocols and regulations. Conduct site visits to verify data accuracy and compliance. Assist in patient recruitment and ensure informed consent procedures. Maintain trial documentation and report findings to stakeholders. Ensure proper handling and storage of investigational drugs. Collaborate with investigators, sponsors, and regulatory authorities. Key Skills: Attention to Detail: Ensuring accuracy in trial data and documentation. Regulatory Knowledge: Understanding of GCP, FDA, and ICH guidelines. Communication Skills: Effective interaction with research teams and sponsors. Problem-Solving: Addressing challenges in trial execution. Project Management: Coordinating multiple aspects of clinical studies. Job Type: Full-time Pay: ₹25,000.00 - ₹40,000.00 per month Benefits: Health insurance Provident Fund Schedule: Day shift Work Location: In person