working as full time clinical data manager

As a research co-ordinator i have been assigned certain responsibilities for monitoring of trail at a site, which include assisting Site Monitoring Visit, Screening of patient based on inclusion criteria, Maintaining the monitoring visit of each patient at site at regular interval, Preparing for Site monitoring visit , Timely and organised reporting of safety issues to the EC, sponsor.

Patient handling during scheduled visits , extensive work on study protocols.Knowledge about epidemiological observational studiesIVRS and IWRS trainedUS-CFRs , ICH-GCP, Schedule Y work

highlighting the various safety issues during conduction of clinical trial, on the basis of site perspective. study the effect of curcumin on liver toxicity caused by the prolonged ingestion of acetaminophen (paracetamol) using mouse model system.biopharmaceutical production for diabetes- a bioinformatics approach (production of plant derieved insulin was developed successfully in safflower plant.)turmeric – an approach as iron chelator or inhibitor in thalassemic patientspresented poster at ISPAT - 10th annual conference of the indian society for prenatal diagnosis and therapy (hepcidine - quantification is a valuable tool for iron balance analysis in thalassaemia)attended conference on jaundice-myths and facts by dr. mahesh kumar goenka and on breast cancer by eminent oncologist at apollo hospitals, kolkata.workshops attended at vanta biosciences, chennai on pre-clinical testing.attended sensitization workshop on emerging trends in epidemiology and basic statistics at national institute of epidemiology, and indian council of medical research,chennai attended endocon 2012 conference, organised by society of gastro intestinal endoscopy of india.secured 1st rank in the POST GRADUATE CERTIFICATE IN CLINICAL RESEARCH

Date of Birth : 27th June Languages Known : English , Hindi , Bengali Permanent Address:BARASAT (KOLKATA)E-Mail: payal6724@gmail.com