I'm a pharmacist with 5+ years of experience in healthcare, pharmaceutical manufacturing, and clinical research. I specialize in medical data abstraction, research support, and regulatory documentation—with a strong focus on accurate data entry and compliance.
I’ve worked on projects involving U.S. hospital records in compliance with HIPAA, GCP-aligned clinical trials, and pharmaceutical quality assurance and quality control under PIC/S GMP and ISO standards. I’m detail-oriented, adaptable, and capable of working independently to deliver high-quality results.
I can support a wide range of tasks—from basic administrative work like handling emails, creating presentations, Excel-based tracking, and document management to complex technical work such as consulting on pharmaceutical laboratory operations, managing stability programs, supporting clinical research, and abstracting clinical data.
What I Offer
- Medical record abstraction & data entry (SEP-1, STS)
- Clinical research & trial support (EDC, eCRF reviews)
- Regulatory/QA documentation & admin tasks
- File/data organization using Notion, Google Workspace, MS Office
Tools & Applications I've used: Microsoft Office, Google Workspace, Notion, Cerner PowerChart, Clinflash, IQVIA RDC, Q-Centrix, REDCap, Intelex, Canva