Dedicated to advancing patient safety and clinical excellence by delivering precise drug safety solutions, comprehensive pharmacovigilance services, and expert medical writing with integrity

With years of experience in drug safety, pharmacovigilance, and quality control, I am committed to ensuring patient safety and regulatory excellence. My values—integrity, precision, and innovation—guide my work in managing adverse event reporting, regulatory compliance, and clinical research. One of my most rewarding moments was streamlining workflows for a large-scale clinical trial, resulting in improved efficiency and compliance. Outside of work, I enjoy spending quality time with my husband and our beloved dog, reading, exploring global cuisines, and engaging in volunteer activities that support community health initiatives. These hobbies reflect my curiosity, attention to detail, and dedication to making a positive impact both professionally and personally.

Work Terms

I am available Monday to Sunday, 9:00 AM to 6:00 PM (MST). Flexible hours can be arranged for urgent projects or time-sensitive deadlines.


Billing Cycle: Payment is expected upon completion of milestones or within 7 days of invoice issuance.

Deposit: A 30% upfront deposit is required for large-scale projects or ongoing contracts.

Preferred Communication Style:

Primary Communication Channels: Electronic communication and Zoom for detailed project discussions, updates, and deliverables.

Response Time: I aim to respond to all inquiries within 24 hours.

Updates: Scheduled updates and progress reviews can be arranged as needed for transparency and alignment.

I’m committed to being responsive and accommodating to meet your project needs efficiently!