Prateep Mittapally

About Prateep Mittapally

I had total 14+ yrs of experience in clinical Research as a Study Coordinator, Sr. eTMF Specialist trained in ICH GCP from various Sponsors. As a ACML I have Start up phase study and end of study delivery, also conduct phase studies. Start Phase Studies will give more confidence to handle any kind of situation in the project because will involve from the begining, SFQ, PSSV, then handle the sites to get ready for SIV process for enrollment. collaboration with all rest of the departments effectively then only will get every stage output achieve on time. Maintain Site communication enrollment process CTMS oversight IP Maintainance key task over the study IRB/ IEC Data Entry (eCRF) Risk Mitigations process throughout the study EAC for concern department to give exact visibility Safety AE\'s n SAE\'S PD maintainance eTMF metrics maintainance Payments for Site Visit Activities third party vendors apart from this many other tasks needs to be performed Monitor the study activities timely manner, this will helps us to avoid study deviations.

Experience

1. Centralized Monitor

   IQVIA

   Sep 2019 — Present · Bangaon, IN

Education

• PRBMSS KORUTLA

  Bachelor of Science (BSc)

  2003 — 2005

Skills

• Oracle Rdc
• Clinical Research Experience
• Medidata
• Impulse Control Disorders
• Site Initiation
• Healthcare
• Sas Programming
• Clinical Research
• Pharmacovigilance
• Sas
• I-Review
• Study Reports
• Clinical Trials
• Protocol Designing
• Fda
• Ecrf
• Icfs
• Pharmaceutical Industry
• Ocd
• Phase Forward Inform
• Data Analysis
• Data Management
• Datatrak
• Epidemiology
• Sql
• Investigator Brochures
• Ba/Be Studies
• Major Depressive Disorder
• Csrs
• Generalized Anxiety
• Ich-Gcp
• Subject Recruitment
• Oc Rdc
• Study Coordination
• Clinical Data Management
• Remote Data Capture
• Feasibilities
• Panic Disorder
• Lifesciences
• Icmr Guidelines