I'm a graduating MD (August 2026) and GCP-certified Clinical Research Coordinator based in Manila, Philippines, with 3+ years of hands-on experience supporting Phase 2–3 multi-center clinical trials for sponsors including Sequirus UK, Wantai Beijing Biological Pharmacy, and Kintor Pharmaceutical Limited.
What I bring to your trial or practice:
Clinical Research
Proficient in Medidata Rave, Clinflash, and InForm EDC platforms
Experienced in SAE reporting, query resolution, source document verification, patient enrollment, randomization, and sponsor/PI coordination
GCP-certified (NIDA Clinical Trials Network) with additional IQVIA certificates in eConsent, InForm Data Entry, and SAE Reporting
HIPAA-trained and experienced in confidential ePHI handling
Remote Medical Scribing
Familiar with Epic, Cerner, and Aprima from my US clinical internship at LoCicero Health (Tampa, Florida)
Strong medical documentation skills across Internal Medicine, Surgery, Pediatrics, OB-GYN, and Emergency Medicine
Fast, accurate real-time charting with deep clinical vocabulary built through medical school and internship
Data & Admin
Experienced with prior authorization workflows (WinFertility, eIVF, UHC claims)
Excel database management for clinical research data
Precise, detail-oriented documentation aligned with regulatory standards
I'm available for remote contracts with US, UK, and international clients. As a Philippine-based professional, I work flexible hours to accommodate US time zones and understand the expectations of Western healthcare environments from direct experience.
Looking for: Remote CRC roles, remote medical scribing positions, clinical data entry/query resolution contracts, and medical virtual assistant engagements. Open to short-term projects and long-term contracts.
