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Sana Bevanoor

B.Pharm Graduate | Pro Advance Diploma in Clinical Research | Pharmacovigilance & Clinical Research Enthusiast | Drug Safety | AE/SAE Reporting | ICH-GCP

Bengaluru

1+ year of work experience

LLRI - Learning Labb Research Institute
Oct 20259 mosPresent

Karnataka, India

Assisted in ICSR processing and ADR reporting Worked with MedDRA terminology Learned ICH-GCP guidelines and clinical trial workflow Supported CRF documentation and informed consent process Gained exposure to regulatory documentation (CTD basics)
LLRI, Bengaluru
Oct 20256 mosMar 2026

1. Interpreted clinical trial protocols to design study visit calendars and schedules per sponsor requirements 1. Designed and developed CRFs/eCRFs ensuring protocol compliance and data integrity standards 1. Worked on EDC platforms and CTMS for data entry, tracking assignments, and project delivery 1. Maintained TMF/ISF documentation; supported AE/SAE reporting per ICH-GCP guidelines 1. Coordinated patient recruitment, ICF process, screening, and follow-up management
Apollo Hospitals
Feb 20251 yrJan 2026

Dispense and review prescribed medications accurately according to hospital protocols. Counsel patients on correct medication usage, side effects, and storage. Maintain detailed pharmacy records and ensure compliance with regulatory standards. Collaborate with doctors and nurses to ensure safe and effective patient care. Assist in maintaining inventory and tracking drug utilization.

Education

Rajiv Gandhi University of Health Sciences (RGUHS)

Bachelor of Pharmacy, Pharmacy

Rajiv Gandhi University of Health Sciences (RGUHS)

20213 yrs2024

Pro Advance Diploma in Clinical Research, Intern

LLRI -Learning Lab Research Institute

20251 yr2026

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Headline

B.Pharm Graduate | Pro Advance Diploma in Clinical Research | Pharmacovigilance & Clinical Research Enthusiast | Drug Safety | AE/SAE Reporting | ICH-GCP

About

I am a motivated B.Pharm graduate with a Pro Advance Diploma in Clinical Research, interested in Pharmacovigilance, Clinical Research, and Drug Safety. I have knowledge of ICH-GCP guidelines, AE/SAE reporting, ADR processing, clinical trial documentation, informed consent process, and safety databases. I am eager to begin my career in the pharmaceutical industry where I can apply my academic knowledge, communication skills, and attention to detail while learning and growing professionally. 📍 Open to work: Bengaluru / Pune / Hyderabad 📩 Open for referrals and opportunities

Location

Bengaluru

Work experience

Intern at LLRI - Learning Labb Research Institute, Oct 2025 - Present · 9 mos, Karnataka, India, Assisted in ICSR processing and ADR reporting Worked with MedDRA terminology Learned ICH-GCP guidelines and clinical trial workflow Supported CRF documentation and informed consent process Gained exposure to regulatory documentation (CTD basics)

Clinical Research at LLRI, Bengaluru, Oct 2025 - Mar 2026 · 6 mos, 1. Interpreted clinical trial protocols to design study visit calendars and schedules per sponsor requirements 1. Designed and developed CRFs/eCRFs ensuring protocol compliance and data integrity standards 1. Worked on EDC platforms and CTMS for data entry, tracking assignments, and project delivery 1. Maintained TMF/ISF documentation; supported AE/SAE reporting per ICH-GCP guidelines 1. Coordinated patient recruitment, ICF process, screening, and follow-up management

Hospital Pharmacist at Apollo Hospitals, Feb 2025 - Jan 2026 · 1 yr, Dispense and review prescribed medications accurately according to hospital protocols. Counsel patients on correct medication usage, side effects, and storage. Maintain detailed pharmacy records and ensure compliance with regulatory standards. Collaborate with doctors and nurses to ensure safe and effective patient care. Assist in maintaining inventory and tracking drug utilization.

Education

Bachelor of Pharmacy, Pharmacy, Rajiv Gandhi University of Health Sciences (RGUHS)

Pro Advance Diploma in Clinical Research, Intern, LLRI -Learning Lab Research Institute

Sana Bevanoor - Intern in Bengaluru | Tal