I'm a Pharmacovigilance and Drug Safety professional based in Edmonton, with 2+ years of experience supporting global clinical and post-marketing safety operations within CRO environments. I have deep knowledge of pharmacology. I have excellent writing skills, I have two review publications and also wrote various book chapters on diabetes and obesity, neurodegenerative diseases like Alzheimer's disease, Parkinson disease. I specialize in ICSR processing, AE/SAE assessment, MedDRA coding, safety narratives, and regulatory reporting, with a strong working knowledge of ICH-GCP, ICH-GVP, Health Canada, FDA, and EMA requirements. I thrive in collaborative CRO settings, delivering high-quality safety documentation and regulatory submissions, and I am aPermanent Resident of Canada authorized to work full-time with no restrictions.

Simran Rana

I'm a Pharmacovigilance and Drug Safety professional based in Edmonton, with 2+ years of experience supporting global clinical and post-marketing safety operations within CRO environments. I have deep knowledge of pharmacology. I have excellent writing skills, I have two review publications and also wrote various book chapters on diabetes and obesity, neurodegenerative diseases like Alzheimer's disease, Parkinson disease. I specialize in ICSR processing, AE/SAE assessment, MedDRA coding, safety narratives, and regulatory reporting, with a strong working knowledge of ICH-GCP, ICH-GVP, Health Canada, FDA, and EMA requirements. I thrive in collaborative CRO settings, delivering high-quality safety documentation and regulatory submissions, and I am aPermanent Resident of Canada authorized to work full-time with no restrictions.

Available to hire

I’m a Pharmacovigilance and Drug Safety professional based in Edmonton, with 2+ years of experience supporting global clinical and post-marketing safety operations within CRO environments. I have deep knowledge of pharmacology.

I have excellent writing skills, I have two review publications and also wrote various book chapters on diabetes and obesity, neurodegenerative diseases like Alzheimer’s disease, Parkinson disease.
I specialize in ICSR processing, AE/SAE assessment, MedDRA coding, safety narratives, and regulatory reporting, with a strong working knowledge of ICH-GCP, ICH-GVP, Health Canada, FDA, and EMA requirements.

I thrive in collaborative CRO settings, delivering high-quality safety documentation and regulatory submissions, and I am aPermanent Resident of Canada authorized to work full-time with no restrictions.

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Work Experience

Drug Safety Associate at Parexel International
September 1, 2024 - October 1, 2025
Processed ICSR, AE/SAE assessments, MedDRA coding, safety narratives, and regulatory submissions, ensuring QA and compliance with ICH-GCP/GVP guidelines.
Trainee Specialist – Pharmacovigilance at Pharma Lex (Cencora)
June 1, 2023 - August 1, 2024
Supported case intake, data entry, follow-ups, and quality checks; assisted with data reconciliation and case triage.

Education

Master of Pharmacy (Pharmacology) at Chitkara University
January 11, 2030 - January 12, 2026
Bachelor of Pharmacy at Swami Devi Dyal College of Pharmacy
November 30, 2026 - January 12, 2026

Qualifications

Add your qualifications or awards here.

Industry Experience

Healthcare, Life Sciences, Professional Services