Clinical Research Coordinator

Job Description Role & responsibilities Data collection for IRIS (includes quality monitors). Participating in the trials and studies performed in the ICUs. Consenting, randomising, monitoring study participants. Reporting adverse events and deviations. Submitting monthly ICU stats as required by the Critical Care Department. Assistance with the academic submissions. Typing and dispatch of reports. Placing purchase order & stock maintenance of chemicals and consumables. Maintenance and calibration of equipments at regular intervals. Maintain QC, EQAS records. Need to take care of all other works which is assigned by the Manager. Reporting to Head of the Department. Preferred candidate profile Qual - BDS, M.Tech Molecular Medicine 1+ years in healthcare. Analytical mindset. Attention to detail. Exceptional interpersonal skills. Outstanding written and verbal communication. Excellent organizational skills. Willingness to continually self-educate. Perks and benefits As per Market standard