Clinical research

Job Description

Site Monitoring: Conducting regular visits to research sites, including hospitals and research institutions, to ensure compliance with protocols and regulations. Data Management: Overseeing data collection, documentation, and verification to ensure accuracy and reliability, often inputting data into databases. Protocol Adherence: Ensuring all aspects of the trial are conducted according to the approved protocol, including patient enrollment, drug administration, and follow-up. Regulatory Compliance: Maintaining awareness of regulatory guidelines (e.g., Good Clinical Practice) and ensuring that the study meets all requirements. Communication and Collaboration: Working with various stakeholders, including researchers, ethics committees, and sponsors, to facilitate the study's smooth operation. Risk Management: Identifying and mitigating potential risks to study participants, data integrity, and regulatory compliance. Reporting: Preparing reports on study progress, including data analysis and potential issues, to inform sponsors and regulatory bodies. Trial Closure: Participating in the process of closing down a trial, ensuring all data is properly archived and reported. Job Types: Full-time, Permanent, Fresher Pay: ₹12,826.83 - ₹38,108.28 per month Benefits: Provident Fund Schedule: Day shift Work Location: In person