Clinical Research Coordinator

A Clinical Research Coordinator is responsible for overseeing the trouble-free running of clinical trials, collecting data obtained from research, coding, and analyzing it. They manage budgets set aside for research and communicate with participants regarding study objectives. Administering questionnaires and monitoring participants to ensure they adhere to the study's rules is also part of their duties. The Coordinator liaises with laboratories regarding research findings and monitors the study to ensure it complies with protocols, is ethically-conducted, and follows regulatory standards. They are responsible for maintaining research records of study activity, including case report forms, drug dispensation records, or other regulatory forms as per FDA guidelines. Directing the collection, labeling, storage, and transport of all specimens is also a key responsibility. The Coordinator ensures that all equipment and supplies needed for the study are in-stock and in good working order. This role may include job types such as Full-time, Permanent, and Fresher. The benefits offered may include Health insurance, Provident Fund, and Work from home options. The schedule may involve Day shift and Morning shift timings. Additionally, there may be performance bonuses and yearly bonuses associated with this position.,