Ihuoma Ogbuokiri

-Managed a panel of 14 to 18 patients daily , making independent diagnostic and treatment decisions while supervising junior resident and coordinating multidisciplinary care.

-Led daily rounds and made clinical decisions in high acuity settings

-Coordinated care with multidisciplinary teams( nursing,pharmacy , specialist)

-Ensured adherence to clinical guidelines and patient safety standards

-Led code blue and rapid response team activations , directing resuscitations efforts.

-Managed ICU/ Critical care patient under the supervision of the Intensivist.

-Assisted in various diagnostic procedures, enhancing procedural skills and patient comfort.

-Engaged in continuous medical education through workshops and conferences to stay updated on best practices in internal medicine.

-Developed strong rapport with patients, earning high marks on patient satisfaction surveys while maintaining strict confidentiality standards.

• Coordinated patient recruitment and retention strategies to enhance study participation.
• Managed regulatory submissions, ensuring compliance with institutional and federal guidelines.
• Developed and maintained study protocols, facilitating effective communication among research teams.
• Monitored participant progress, documenting data collection and addressing any issues promptly.
• Implemented quality control measures to enhance data accuracy throughout research studies.
• Screened patient records, databases, and physician referrals to identify prospective candidates for research studies.
• Gathered, processed, and shipped lab specimens.
• Followed informed consent processes and maintained records.
• Assessed patients'' eligibility criteria following strict adherence to inclusion/exclusion guidelines.
• Managed patient recruitment, informed consent process and data entry to support trial objectives.
• Participated in initiation visits and investigator meetings, implementing trials following study timelines and budgets.

• Assisted in managing clinical trial documentation and regulatory compliance processes.
• Coordinated participant recruitment efforts, ensuring adherence to ethical standards and guidelines.
• Conducted literature reviews to support study design and protocol development initiatives.
• Collaborated with multidisciplinary teams to streamline data collection and analysis procedures.
• Enhanced patient enrollment for clinical trials through effective communication with potential participants.
• Reduced errors in data entry by performing thorough quality control checks on entered data from source documents.
• Contributed to successful clinical research projects by efficiently managing multiple tasks in a fast-paced environment while maintaining attention to detail.

• Developed and implemented engaging lesson plans aligned with curriculum standards.
• Facilitated classroom discussions to enhance student understanding and participation.
• Assessed student performance through various evaluation methods to ensure learning outcomes.
• Collaborated with colleagues to refine teaching strategies and share best practices.