Rishit Bagadia

About Rishit Bagadia

As a dedicated PharmD candidate, I\'m eager to leverage my comprehensive background to drive positive change in the pharmaceutical field. My five-year academic journey at RK University, Rajkot, has provided a robust foundation in pharmaceuticals and healthcare.Complementing my formal education is two years of practical experience as a pharmacist at a medical store, where I honed skills in patient counseling, medication management, and interpersonal communication. I\'ve also enhanced my practical skills through month-long internships at three hospitals, exposing me to various clinical settings and healthcare systems.To further broaden my expertise, I\'ve completed five specialized certificate courses, demonstrating my commitment to lifelong learning. Currently, I\'m gaining hands-on experience as a Clinical Pharmacist at HCG Hospital Ahmedabad.With a strong academic background and a passion for advancing healthcare, I\'m interested in clinical research. I\'m pursuing a clinical research course at Cliantha Academy, deepening my knowledge of regulatory guidelines, drug development, and trial management.As I near the completion of my PharmD program, I\'m seeking opportunities in clinical research organizations and pharmaceutical companies. My skills in pharmacovigilance, regulatory affairs, and clinical trial operations make me a strong candidate for roles in clinical research.I\'m excited to collaborate with like-minded professionals who share my passion for advancing healthcare research. Together, let\'s shape the future of healthcare research and contribute to innovative treatments and therapies that improve patient outcomes.

Experience

1. Project Coordinator

   Cliantha Research Limited

   Jun 2025 — Present · Ahmedabad, IN

   As a Project Coordinator at Cliantha Research, my role involves ensuring compliance with protocols, SOPs, and regulatory requirements for clinical studies. Key responsibilities include- Coordinating study activities (e.g, informed consent, dosing, sample collection)- Ensuring timely compliance with sponsor requirements- Preparing clinical updates and submissions to Ethics Committee and sponsors- Maintaining Trial Master File and generating deviation reports- Reviewing documents (e.g, CRFs, ICFs) and resolving queries- Providing responses to sponsor observationsI\'m responsible for ensuring the smooth conduct of studies, data quality, and regulatory compliance.

Education

• RK University

  Doctor of Pharmacy - PharmD, Clinical pharmacy

• Cliantha Academy

  Clinical Research, Certificate Course

• Saint Xavier's school Botad

  High school

• Gyanmanjari Vidhyapith

  12th Board, Secondary High school