Asit Behera Email and Phone Number

1.Maintained compliance with protocols covering patient care and clinical trial operations. 2.Screened patient records, databases, and physician referrals to identify prospective candidates for research studies. 3.Followed informed consent processes and maintained records. 4.Gathered, processed, and shipped lab specimens. 5.Worked with principal investigator and sponsors to facilitate daily trial activities and comply with research protocols. 6.Participated in initiation visits and implementing trials in accordance with study timelines and budgets. 7.Collected data and followed research protocols, operations manuals, and case report form requirements. 8.Developed and maintained accurate and up-to-date case report forms and source documents. 9.Monitored patient safety throughout clinical trials and reported any adverse events. 10.Coordinated and monitored clinical trial activities to support timely and accurate completion of studies. 11.Collaborated with clinical staff and other healthcare professionals to support clinical trial data accuracy. 12.Followed clinical research protocols and conducted study visits in compliance with ICH/GCP and FDA regulations. 13.Monitored unit budget to meet financial objectives for spend rate and funding.

• Worked with IPD, OPD, OT & medical receiving departments to provide medications for patients of all age groups.• Handled stock and order supplies of medicines and drugs. • Resolved queries regarding dosages, indications and drug availability.• Protected drug inventories from expiry date.• Checked medication bottles for proper labeling before allocating to patients.

• Handling done instruments like GC,HPLC,DSC,KF titrator,Polarimeter, FTIR and U.V visibible spectrophotometer.

Worked in manufacturing department - tablet, capsules and syrup section.• Maintained proper drug storage procedures, registries and records for controlled drugs.

Basic Hospital training and Drug distribution.