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About Candidate
A Clinical Research Coordinator with a double major in Biochemistry and Genecs and experience working with paents in person and virtually in the medical and scienfic fields. An aspiring MD or PA with varied paent care experience including primary care, obstetrics, pediatrics, gynecology, women’s health, oncology and clinical trials experience in cardiology, nephrology, and podiatry. Supports research studies by collecng data, providing administrave support and accurate documentaon. Complies with regulaons and process procedures and ethical guidelines. Experience includes effecvely communicang with healthcare professionals and study parcipants.
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Work & Experience
• Managed mulple oncology clinical trials in compliance with study protocols and regulatory melines. • Performed accurate, mely data entry into EDC systems and maintained complete source documentaon. • Maintained ongoing communicaon with sponsors, invesgators, and cross-funconal teams. • Ensured regulatory compliance with GCP and instuonal guidelines.
• Manage all aspects of clinical trials, including subject recruitment, eligibility verificaon, informed consent, data collecon, sample collecon, and compliance with protocol and regulatory requirements. • Ensure accurate documentaon, data entry, and secure handling of subject informaon while maintaining compliance with federal regulaons and study protocols. • Support sponsor visits, audits, and inspecons, resolve queries, and ensure mely reporng and compliance with electronic data capture (EDC) requirements.
Supported various research pertaining to psychological/behavioral studies and brain smulaon using tDCS to improve mental health in people suffering from severe mental illness. • Collected data by conducng research interviews and tesng of biological samples. • Recruited and screened subjects for research studies according to IRB protocols. • Developed protocol manuals, responded to individual’s quesons and established database files and report to ensure proper documentaon and accuracy.
