Deep Maurya

Responsible for all aspects of study site initiation visits, routine monitoring and conduct of pre-study and close-out of clinical sites. IP accountability and availability, tracking and management of all Clinical Trial Conduct of monitoring visits as per monitoring plan to check compliance with study management, protocol & other requirements at all assigned sites. The overseeing Progress of Clinical trials and ensuring that it is conducted, recoded, and reported in accordance with protocol, SOP, ICH-GCP