Anshul Sharma

I’m a collaborative, results-oriented professional seeking opportunities in Clinical Research and Data Management. I bring deep understanding of clinical trial coordination, data collection, clinical data management, and regulatory compliance, with knowledge of ethical standards and legal requirements such as 21 CFR Part 11, ICH-GCP, and HIPAA.

I’ve supported safety and pharmacovigilance activities, including ADR reporting, signal detection, risk management, and aggregate safety reporting (DSUR, PSUR, PBRER, ASR), using safety databases such as ARGUS and MedDRA. From my internship experience in medical device complaint management at Cognizant to my research roles as Research Assistant and Senior Research Fellow—including hands-on eTMF management—I consistently deliver accurate records, clear reporting, and documented SOPs, and I’ve published 4 research papers.