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Clinical research

0 years

0 Lacs

Chennai, Tamil Nadu

Posted:2 months ago| Platform: Indeed logo

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Skills Required

research monitoring compliance regulations data management documentation verification reliability enrollment communication collaboration ethics risk integrity reporting reports analysis schedule

Work Mode

Work from Office

Job Type

Full Time

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

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