Hari y

About Hari y

I am a physician (MBBS) with over 4 years of clinical and research experience across hospital settings and clinical trial operations. My background spans ICU patient care, pharmacovigilance, adverse event reporting, and regulatory-compliant clinical trial documentation aligned with ICH-GCP, FDA, and EMA standards. After relocating to the United States in late 2023, I spent time completing my work authorization process while continuing to build on my clinical research knowledge reviewing EDC workflows, query resolution, SAE/AE reporting practices, and eTMF documentation standards. I am now fully authorized to work in the US and actively seeking entry-level to mid-level roles in Clinical Research Coordination (CRC), Clinical Trial Administration (CTA), CRA where I can immediately contribute using both my medical training and research background. My physician background gives me a practical edge I understand protocols, patient safety, and clinical data not just as procedures, but from real bedside experience. Open to on-site, hybrid, and remote opportunities across the US.

Experience

1. Opentowork

   Aug 2025 — Present · Raleigh-Durham-Chapel Hill, NC, US

   Since receiving US work authorization in August 2025, I have been actively pursuing clinical research opportunities while continuing structured professional development in US clinical trial operations.Key activities during this period include:Reviewing FDA, ICH-GCP, and EMA regulatory frameworks applicable to US clinical trialsPracticing EDC workflows, CRF review, query resolution, and data reconciliation processesCompleting GCP certification through NIDA Clinical Trials Network (valid through 2028)Actively networking with CROs, research sites, and clinical professionals across North CarolinaApplying and interviewing for CRC, CTA, and Drug Safety Associate roles

Education

• Kunming Medical College

  Bachelor of Medicine, Bachelor of Surgery - MBBS, Medicine