About
I am a recent B.Pharm graduate with a strong interest in Clinical Research and Pharmacovigilance. I have completed training in ICH-GCP, Good Clinical Practice, Pharmacovigilance, Clinical Research, and Project Management for Clinical Research Professionals. I have a basic understanding of ICSR processing, ADR/SAE reporting, drug safety, clinical trial documentation, and GVP principles. I am seeking an opportunity to gain practical industry experience and develop hands-on skills in clinical research and pharmacovigilance. I am particularly interested in clinical trial coordination, clinical research operations, patient safety, and drug safety. I am a quick learner, detail-oriented, and eager to contribute while continuously developing my professional skills.
Education
- 2026
