Very good experience and expertise in Managing clinical trials of different phases from phase II to phase IV.Overall 5 years of experience As aSr. CRA, CRA, CTA, CRC and Site Management.Around 2 years of Senior CRC experience with many multinational companies.1 Year of experience as CRC.Affiliated Member of Institute of Clinical Research (ICR), UK.Certified in “Understanding FDA And The FDA Approval Process ”, Delevered by Dr. Joshua Sharlin, USA (Former US FDA Reviewer).Very good hand over MS office and internet use.Specialties: Site Management skills.Good Knowledge of Regulatory Affairs in India, UK and USA.Good Knowledge of ICH-GCP, Schedule Y, ICMR Guidelines, Pharmacovigilance.Good Knowledge of Protocol Designing, Case Report Form, Informed Consent Forms..