kasim bhimani

I am a regulatory affairs specialist with experience reviewing clinical research protocols and managing regulatory documentation for phases I–IV trials. I ensure compliance with ICH and GCP guidelines and support investigators through IRB submission processes.

At Methodist Health System Clinical Research Institute, I obtain and track regulatory documents, prepare protocol and consent amendments, and assist coordinators with adverse event identification and reporting. I also develop and adapt informed consent documents and facilitate the informed consent process for investigators.

In parallel, I work as a sales specialist at Apna Bazaar where I build and grow customer accounts, prospect for new business, close incoming leads, and represent product offerings through on-site meetings and cold outreach. I contribute to sales growth through product knowledge and relationship-building.

My background includes a B.S. in Biology from the University of North Texas and prior medical school coursework at William Carey College of Osteopathic Medicine. I combine regulatory rigor with client-facing communication to support clinical research and business development goals.