Clinstinct Clinical Research

Bhubaneswar, Odisha

Overseeing the trouble-free running of clinical trialsCollecting data obtained from research, coding and analyzing itManaging budgets set aside for researchCommunicating with participants regarding study objectivesAdministering questionnaires and monitoring participants to ensure they adhere to the studys rulesLiaising with laboratories regarding research findingsMonitoring the study to ensure that it complies with protocols, is ethically-conducted and follows regulatory standardsMaintaining research records of study activity, including case report forms, drug dispensation records or other regulatory forms as per FDA guidelinesDirecting the collection, labeling, storage and transport of all specimensMaking sure that all equipment and supplies needed for the study are in-stock and in good working order

A pharmacovigilance associate ensures compliance with applicable regulations or standard operating procedures; specialises in drug safety management, clinical trials and medical supervision. Responsible for conducting, monitoring or reporting regular pharmacovigilance developments and supervising the processes related to ensuring drug effectiveness and avoiding adverse effects or side effects of marketed pharmaceutical products among the general population in research trials and hospitals.Pharmacovigilance associate aim at reducing the risks associated with administering and prescribing drugs along with improving safety and treatment outcome in patient care. The role includes activities of important case report follow-up; processing and writing adverse event programs; serving link between the company, healthcare experts and patients for delivery of valid information on product safety; Conducting and supervising regular pharmacovigilance processes; attending several product safety meetings and adding functionality to product sa