ONYEBUCHI NWAOKOLO DNP

• Collaborated closely with thePrincipal Investigator (PI) in planning, implementation, and management of clinical research studies, ensuring adherence to study protocols and regulatory requirements.
• Administered study interventions, treatments, and medications as prescribed, monitoring participants for adverse events and ensuring participant safety throughout study duration.
• Assisted in screening, recruitment, and enrollment of study participants, conducting thorough assessments to determine eligibility and obtain informed consent.
• Improved patient outcomes by implementing evidence-based care and treatment plans tailored to individual needs.
• Decreased hospital readmissions by providing thorough discharge education and follow-up care coordination.
• Performed comprehensive physical assessments, accurately diagnosing conditions, and determining appropriate interventions.
• Managed acute and chronic illnesses, developing personalized treatment plans that addressed patients'' unique needs.
• Optimized clinic operations, contributing to improved patient access and reduced wait times for appointments.
• Handled complex cases involving multiple comorbidities effectively by employing critical thinking skills and seeking expert consultations when necessary.
• Ordered and interpreted diagnostic tests to develop and implement treatment plans.
• Enhanced patient satisfaction through effective communication, empathy, and timely response to concerns.

Pre-Study

• Order specialized equipment for special clinical studies
• Oversee the informed consent process of study participants
• Perform screening examinations
• Review subject screening data, including subject medical histories; ECGs; radiographic studies; laboratory studies; lab work, and any other ancillary tests required per study protocol
• Interact with study participants in person on-site or via written, electronic, or telephone correspondence to address any screening-related questions
• Interact with study participants regarding safety concerns at on-site visits or screening reviews
• Review potential study participant’s eligibility based on protocol inclusion and exclusion criteria
• Approve study participants for inclusion in the clinical trial study

During Study

• Review, initial, and date all safety-related data in a timely manner, including laboratory studies, ECGs, and all other safety data as dictated by the study protocol
• Safety Monitoring: Monitor, review, and track adverse events and serious adverse events, providing treatment as needed.

Post-Study

• Safety Monitoring, perform end-of-study physical examinations, and provide follow-up for any ongoing adverse events and serious adverse events
• Assist Principal Investigator/Director of Clinical Research with on-site client review of Case Report Forms
• Responsible for adverse drug assessments, evaluations, and documentation under the guidance of the Principle Investigator
• As needed, assist with clinic associate’s training on ECG procedures, manual vital sign procedures, and assessment skills related to reporting adverse events

• Improved patient outcomes by conducting thorough psychiatric assessments and developing personalized treatment plans.
• Reduced hospital readmissions through providing effective psychotherapy and medication management for patients with mental health disorders.
• Enhanced interdisciplinary collaboration by participating in regular team meetings to discuss patient progress and adjust treatment strategies as needed.
• Educated patients and families on mental health conditions, coping strategies, and community resources for support.

• Improved patient outcomes by implementing evidence-based care plans and collaborating with interdisciplinary teams.
• Reduced urgent care wait times through efficient assessment, diagnosis, and treatment of patients with acute illnesses and injuries.
• Prevented hospitalizations by providing timely intervention for chronic disease exacerbations in the urgent care setting.

• Prescribed appropriate pharmacologic and non-pharmacologic treatment modalities to support the health and comfort of patients.
• Improved patient outcomes by implementing evidence-based care and treatment plans tailored to individual needs.
• Enhanced patient satisfaction through effective communication, empathy, and timely response to concerns.
• Contributed to clinical research initiatives, enhancing evidence-based practice within the field of family medicine.

• Submitted accurate documentation, reporting, and in-depth nursing observation to support continuity of total patient care.
• Improved patient outcomes by implementing evidence-based nursing interventions and individualized care plans.
• Reduced hospital readmissions through effective discharge planning, patient education, and follow-up care coordination.
• Streamlined medication administration processes for increased safety and accuracy during busy shifts.

• Educated patients, families, and caregivers on diagnosis and prognosis, treatment options, disease process and management, and lifestyle options.
• Collaborated with interdisciplinary teams to develop comprehensive treatment plans for complex patients with multiple comorbidities.
• Prevented the spread of infections by consistently adhering to strict infection control protocols and educating patients on proper hygiene practices.
• Conducted thorough patient assessments to identify changes in condition, promptly notifying physicians and initiating appropriate interventions when necessary.

• Documented accurate and complete patient information to address patient problems and expected outcomes.
• Performed routine evaluations of each patient's status, needs, and preferences. Obtained patient vital signs and input/output measurements from inpatients.
• Educated patients and families on health promotion, disease prevention, and self-care management strategies.