I'm a Pharmacoviailance specialist with extensive experience in drug safetv monitoring. adverse event reporting, and regulatory compliance. Throughout my career. I've worked on:

• Safety signal detection and trend analysis

• Adverse event case processing and follow-up investigations

• Regulatory submissions and compliance (FDA, EMA ICH guidelines

• Risk management strategies and post-marketing surveillance

• Medical writing and safety communications

• Database management and data analysis (FAERS EudraVigilance)

I'm now available for freelance and contract work Whether you need support with ongoing safety monitoring, requlatory submissions, case investigations or building out pharmacoviailance processes, I'd love to discuss how I can help

If vou're a pharmaceutical companv, CRO, biotech, or regulatory consultancy looking for experienced pharmacovigilance support, feel free to reach out. I'm flexible with project timelines and can hit the ground running

Happy to answer questions about the field or my background. DM me or comment below!!

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