Shubham Ladkat

WORK HISTORY

EDUCATION

ABOUT SHUBHAM LADKAT

My expertise includes: • eTMF Management: Organizing, indexing, and maintaining essential trial documents. • Investigational Drug Reconciliation: Ensuring proper tracking and compliance of study drugs. • Study Equipment & (SRTE)Site Activation Support: Managing shipments, tracking enrollment metrics, and coordinating site readiness. • Data & Report Analysis: Generating custom reports, trackers, and visualizations to streamline study deliverables. • Cross-Functional Collaboration: Facilitating communication between study teams, internal staff, and external vendors. • System & Access Management: Handling access requests and ensuring smooth system operations. • Clinical Research Systems Expertise: Proficient in Wingspan, CTMS (Siebel CRM), Medidata RAVE, ELVIS eTMF, Veeva Vault, PhlexEview, Signant Health IRT, DrugDevSpark, and Target EDC, with hands-on experience in Oracle Inform IRT, Cenduit, and Suvoda IRT.With a strong foundation in blinded and unblinded research projects, I am committed to improving clinical trial efficiency and compliance. Always eager to learn and contribute, I look forward to connecting with professionals who share a passion for advancing healthcare and research.Beyond the workspace, I chase open roads, fast machines, and stunning landscapes—fueling my passion for all things on wheels and travel photography. Whether it’s streamlining study processes or capturing the perfect shot on the go, I thrive on precision, speed, and exploration. Let’s connect—whether for clinical insights, road trips, or photography inspiration!#ClinicalResearch #Pharmaceuticals #ClinicalTrials #DataAnalysis #eTMF #CentralizedMonitoring