Detail-oriented Clinical Research Coordinator (CRC) with 3 years of experience supporting Phase I-IV clinical trials across Oncology, Cardiovascular, Infectious Disease, and Pharmaceutical therapeutic areas. Proficient in ICH-GCP E6(R2/R3) guidelines, IRB submissions, eConsent, and regulatory document management. Skilled in Decentralized Clinical Trials (DCTs), hybrid study coordination, and remote patient monitoring. Demonstrated ability to manage multi-protocol site operations, drive subject enrollment, and ensure zero protocol deviations. Dual master's degrees in Health Informatics and Pharmacy, with added competency in medical coding (ICD-10-CM, CPT), EDC platforms, and healthcare data analytics using Power BI.
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