M.

Details

Your skills and interests

Regulatory Compliance: Knowledge of FDA, EMA, and Health Canada regulations
Pharmacovigilance: Adverse event monitoring and reporting, signal detection
Research & Analysis: Clinical data analysis, research methodology
Documentation & Reporting: Safety reports, compliance documentation
Technical Skills: Microsoft Office Suite, pharmacovigilance software (if applicable)

About

Pharm.D graduate with robust expertise in pharmacovigilance and regulatory affairs, and a PEBC
aspirant. Bringing a strong foundation in drug safety, regulatory compliance, and clinical research,
honed through comprehensive study and hands-on experience. Dedicated to supporting
pharmaceutical innovation while ensuring compliance with global regulatory standards, I am
eager to contribute to a forward-thinking pharmaceutical organization committed to patient safety
and quality.
• Proficient in regulatory standards and guidelines (e.g., ICH-GCP, TCPS 2: CORE-2022).
• Skilled in monitoring adverse events, ensuring compliance, and collaborating
cross-functionally to support patient safety.
I am available to work full-time, part-time, or on a volunteer basis, depending on your needs.
Additionally, I am open to relocating to another city or province if required, ensuring I can fully
contribute to your team and gain the experience necessary for my professional development.
Pharmacists’ Gateway Canada ID: 8334-713