Muzammil Khan
Certified Clinical Drug Development Professional | Clinician Turned Non-clinical Professional Professional | Drug safety and Pharmacovigilance Professional | Skilled in Safety Monitoring and ADR reporting
Bengaluru
1+ year of work experience
Jun 20262 mosPresent
Hyderabad, Telangana, India
Assisted in understanding the clinical drug development pathway, including clinical trial phases, study design, drug safety, and regulatory documentation. Reviewed research articles, protocol samples, clinical study reports, drug profiles, and safety references to prepare concise academic summaries. Supported development of clinical research learning resources, including case-based exercises, training slides, webinar notes, and student reference materials. Gained exposure to informed consent, ethics committee submissions, subject safety, adverse event documentation, ICH-GCP guidelines, and trial documentation. Participated in practical assignments related to pharmacovigilance workflows, clinical data review, medical writing, and study coordination basics.
Jun 20251 yrMay 2026
Mar 20251 yr 2 mosApr 2026
Bangalore Urban, Karnataka, India
Rotated through major clinical specialties including Medicine, Surgery, Pediatrics, Obstetrics & Gynecology, Emergency Medicine, and Community Medicine.
Assisted in patient assessment, diagnosis, treatment planning, and follow-up care under supervision.
Performed routine clinical procedures including venipuncture, IV cannulation, catheterization, wound dressing, and sample collection.
Participated in emergency and critical care management, including triage and basic life support.
Education
Bachelor of Medicine and Surgery, Medicine
North caucasian state academy
20186 yrs2024
Executive Program in Clinical Drug Development, Clinical and Industrial Drug Development
Academically Global
20262026
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