Elizabeth Safari Lubembe

• Vaccine cold chain management check VVM and fridge temperature daily, follow infection prevention measures.
• Provide health education on vaccines use, risk assessment and Vaccination of clients according to travel requirement of destination country. Managed to vaccinate more than 2000 clients who are on resettlement.
• Weekly Update, monitoring and replacement of items consumed in the emergency trolley.
• Vaccine stock management stock and order from Vaccine unit team in regional office.
• Client education on vaccine side effects that is MMR, TD, Oral Polio, hepatitis, yellow fever meningococcal and IPV vaccine, emergency management of adverse effects and refer to camp hospital.
• Monitoring and management of outbreaks of polio, cholera, and measles in the camp.
• Monthly vaccine report to IOM Regional office, MHAC Nairobi Pharmacy, Vaccination physicians’ focal point and HSO.
• Training and mentorship of newly recruited nurses on IOM vaccination routine.
• Provided counseling on TB and HIV prevention, treatment, and management.
• Work with panel physician in interpreting HIV and TB lab results.
• Monitor clients on TB and HIV treatment, including sputum tests, X-RAY images, phlebotomy and side effect management.
• Escort migrants for medical reasons as needed to maintain their care during all migration stages.
• Preparation of clients, Risk assessment and evaluation of beneficiaries fit to travel on transit to Nairobi in collaboration with Operations department.
• Data entry of clients in Mimosa an e-medical application as per resettlement country travel requirements.
• Follow ups, Mental health reviews and treatment.
• Collaborated with Psychiatrist and Mental Health Nurse for any applicants who need Psychiatric evaluation and follow up at the Mental Health Unit.
• Follow up on Laboratory for RDS CDT and Psychiatrist for specialist report.
• Administration and referral to other camp hospital.
• Collaborate with panel physician on MHD-I's clinical and administrative tasks and mentor and coach new nurses and interpreters in MHD with MHD Supervisor.
• Maintain collaborative relationships with various partners to facilitate the follow up and relevant information sharing who include Operations, other health providers, panel physicians, embassies, UNHCR and NGO’s.
• Pharmacy stock management.
• Updated stock cards for all pharmacy items and order and dispose of medical supplies and equipment with Nairobi Pharmacists.
• Check the MHAC pharmacy stock, data analysis, and follow up on preparation of medical kits and emergency kits within the MHAC and for medical escorts followed the guideline if applicable.
• PEP KIT Custodian for MHAC .

• Administered life-saving medications and therapies under strict protocols, guiding patients towards recovery from acute illnesses or injuries.
• Monitored hemodynamic parameters and analyzed complex data sets, making appropriate adjustments to treatment plans based on patient response.
• Served as a preceptor for new nurses entering the critical care field, sharing knowledge and expertise to facilitate successful integration into the team.
• Demonstrated a high level of adaptability in adjusting to ever-changing patient acuity levels within the critical care unit, ensuring consistent delivery of safe and effective nursing care.
• Actively participated in continuing education opportunities to remain current with best practices in the rapidly evolving field of critical care nursing.
• Managed multiple priorities simultaneously while maintaining focus on providing exceptional patient-centered care within a fast-paced critical care environment.
• Utilized advanced assessment skills to quickly identify changes in patient condition requiring intervention or escalation of care.
• Provided compassionate end-of-life care for terminally ill patients and their families, ensuring dignity and comfort during difficult times.
• Oversaw various aspects of telemetry by administering pa catheters and arterials, vasoactive drugs, titration, thrombolytic therapy, dysrhythmia interpretation, and chest tubes.
• Provided compassionate end-of-life care, supporting patients and their families during difficult transitions.
• Delivered top-notch care exceeding department, hospital and Joint Commission standards.
• Worked with intubated and ventilated patients, monitoring and reporting on conditions to maintain stats within optimal levels.
• Demonstrated sound clinical judgment when making decisions about patient interventions under rapidly changing circumstances.
• Counseled patients and families on treatments, care options and discharge instructions.
• Provided education to patients and families on critical care conditions, treatment options, and self-care strategies to empower them in their healthcare journey.
• Conducted patient assessments, recorded vitals, and analyzed records and charts to define care requirements.
• Provided targeted care and treatment to critical care patients.

• My main tasks were implementation of WHO sponsored Action clinical trial project at phase 3 in University of Nairobi in Nakuru County.
• A multi country, multi-Centre two arm parallel double-blind placebo controlled randomized trial of antenatal corticosteroids for women at risk of imminent birth in early pre term period in low resource hospital.
• Planning and coordinating study field activities in Nakuru level 5 hospital
• This involved monitoring of adherence and complications to both the mother and the neonate.
• Assisted in developing and enforcement of standard operating procedures and infection prevention strategies for labor ward, newborn unit and theatre in line with MOH guidelines.

Submission of protocol, tools, consent forms and other required documents to Ethics and Scientific Committee and NACOSTI for required approvals and permit.

Coordination of stakeholder engagement meetings with representatives from National, county Ministry of Health, and independent auditors.

• Ensured there was 100% follow up of participants who participated in the program and monitored any adverse events.
• Obtained informed consent for qualitative and quantitative data collection of subject participation, protection of client information.
• Conducted daily data audits of data base(qualitative and quantitative) to ensure completeness and accuracy of data collection, report writing, validation and dissemination
• Timely and accurate data collection and documentation of quality patient information.
• Conduct literature reviews and systematic reviews
• Oversaw up to date documentation approvals of ERC, NACOSTI and pharmacy and poisons board.
• Participated in team project to review and improve maternal critical care unit and neonatal intensive care unit infection prevention process guidelines.
• Ensured timely compliance and submission of daily reports after each activity.
• Conduct daily check in meetings with research assistants to document field experiences and address challenges experienced by Research Assistants.
• Training of research assistants and pretesting of data collection tools.
• Development of knowledge pharmaceutical drugs including scientific manuscripts, policy briefs and blog articles.
• Supported the lead principal investigator in development of manuscripts for publication and other knowledge products
• Participated in site monitoring visits, addressing any concerns or discrepancies related to patient enrollment or data collection procedures.
• Maintained up-to-date knowledge of industry regulations by attending professional development seminars and reviewing relevant publications
• Maintained up-to-date knowledge of industry regulations by attending professional development seminars and reviewing relevant publications regularly.
• Monitored safety events during clinical trials by promptly reporting adverse events and implementing corrective action plans as needed.
• Facilitated efficient organization of study-related documents through meticulous record-keeping practices.
• Educated patients regarding all facets of clinical study participation.
• Developed strong relationships with patients through compassionate care coordination during their participation in clinical studies.
• Improved patient retention rates in longitudinal studies by establishing rapport with participants and maintaining regular follow-up communication throughout trial duration.
• Enhanced patient recruitment by developing targeted outreach strategies and materials for clinical trials.
• Conducted literature reviews to inform study designs and enhance understanding of current trends in clinical research.
• Assisted with research protocol development.
• Supported investigators with the design and implementation of study protocols, ensuring adherence to regulations and ethical guidelines.
• Managed updates and input for patient information database.
• Expedited study progress by overseeing timely completion and submission of required documents, forms, and reports in accordance with regulatory guidelines.
• Managed study databases, ensuring accurate data entry, storage, and retrieval for analysis purposes.
• Coordinated with multidisciplinary teams to facilitate smooth communication between researchers, clinicians, and support staff.
• Submission and follow up of applications for Ethics and Scientific review Committee and NACOSTI in Kenya.
• Knowledgeable in ethical guidelines for research in Kenya as per NACOSTI guidelines.
• Fostered a supportive environment for research participants through empathetic communication and careful attention to their needs during clinical trial enrollment and followup.
• Assisted in the preparation of manuscripts for publication by conducting thorough data analysis and proofreading content for clarity.
• Provided training to new team members on proper procedures for data collection, documentation, and reporting in clinical trials.
• Assisted principal investigators in evaluating treatment outcomes by conducting thorough assessment of patient data.
• Streamlined data collection processes for improved accuracy and efficiency in clinical research projects.
• Demonstrated advanced knowledge of federal regulatory compliance guidelines.
• Collaborated with clinical staff and other healthcare professionals to support clinical trial data accuracy.
• Gathered, processed, and shipped lab specimens.
• Followed clinical research protocols and conducted study visits in compliance with ICH/GCP and FDA regulations.
• Managed patient recruitment, informed consent process and data entry to support trial objectives.
• Maintained accurate and up-to-date case report forms and source documents for traceability.
• Followed informed consent processes and maintained records.
• Collected data and followed research protocols, operations manuals, and case report form requirements.
• Worked with principal investigator and sponsors to facilitate daily trial activities and comply with research protocols.
• Screened patient records, databases, and physician referrals to identify prospective candidates for research studies.
• Developed and maintained accurate and up-to-date case report forms and source documents.
• Coordinated and monitored clinical trial activities to support timely and accurate completion of studies.
• Monitored patient safety throughout clinical trials and reported any adverse events.
• Maintained compliance with protocols covering patient care and clinical trial operations.
• Prepared and maintained regulatory documents for clinical trial submissions.
• Participated in initiation visits and investigator meetings, implementing trials following study timelines and budgets.
• Obtained and documented patient medical history, vital signs and current complaints at intake.
• Updated inventory, expiration and vaccine logs to maintain current tracking documentation.
• Taught patients about medications, procedures, and care plan instructions.
• Collected and documented patient medical information such as blood pressure and weight.
• Supported duties for diagnostic and technical treatment procedures, such as setting up and operating special medical equipment and apparatus.
• Explained procedures to patients to reduce anxieties and increase patient cooperation.
• Conducted monthly and quarterly inventory of supplies for Action Trial study using facility cost reporting records.
• Implemented care and efficiency improvements to support and enhance office operations.
• Collaborated with medical and administrative personnel to maintain patient-focused, engaging, and compassionate environment.

• This was a HIV prevention Program for adolescence girls and young women in the reproductive health.
• I oversaw the Maternal and child health clinic in provision of Ante natal services in pregnant women, family planning services, pre-exposure prophylaxis (Prep) to persons at risk of contracting HIV/AIDS.
• I contributed to the development of HIV section rolling workplan and provided technical and project support.
• Whereby I was able to achieve our targets.
• I was actively involved support the planning and implementation of HIV Network meeting, monthly reporting and quality improvement strategies within MOH.
• I was in charge of training and mentorship of health workers on oral PrEP implementation in facilities collaboration with other partners.
• In Liaison with other partners, I ensured commodity availability and stocking through data base entry.
• I facilitated school health promotion measures by providing school health education preventive measures in hand hygiene, mass polio and measles vaccination, nutritional screening and supplementation and deworming of children.
• I offered guidance and counselling in youth friendly clinics in Maseno university and the surrounding community.
• I developed strategies that ensures the community had access to quality healthcare services through community involvement.
• I was involved in screening and treatment of STI, cancer, Tuberculosis and Gender based violence cases and offered appropriate referral mechanism through collaboration.
• I was part of the team that ensured the successful completion of pre-exposure prophylaxis delivery, uptake and implementation for young women and adolescent program in Kisumu.
• I was also a peer counsellor in the youth friendly clinics and initiated mental health program in the clinics.
• I documented and presented challenges and lessons learnt in delivery and implementation of PrEP at the end of the program.
• I Particularly ensured that we administered public health campaigns and capacity building on immunization, proper nutrition and disease prevention and provided homebased care.

• Assist with Curriculum Development and Teaching
• Assist with preparation of course outlines and course content on gender and reproductive health
• Assist with delivery of training for students, faculty and other relevant stakeholders on gender, social justice and sexual and reproductive health issues
• Assist with grading student assignments and exams
• Mentor, supervise and guide students through their learning as well as ongoing professional growth
• Assist and engage in collaborative Research
• Assist with and partake in research on gender and global health issues
• Used Power point presentation to design training participants
• Identified participants with specific skill sets and assisted in finding solutions to best improve their workplace and implement SRHR training.

• Educated mothers and families on pregnancy-related topics to inform and prepare for pregnancy, childbirth and newborn care.
• Promoted benefits of breastfeeding and offered education on proper positioning, latching and breast care.
• Kept accurate medical records by documenting patient prenatal care, labor and delivery and postpartum care.
• Empowered mothers to make informed decisions about their care through comprehensive education on pregnancy, childbirth, and newborn care.
• Supported families during the grieving process following pregnancy loss or infant death with empathetic emotional support and resource referrals for ongoing counseling services.
• Managed fetal distress and delivery complications calmly to provide safety to mothers and babies.
• Performed neonatal assessments by checking baby's vital signs and performing physical exams to determine overall health at birth.
• Built strong rapport with patients through open communication channels that encouraged feedback and collaboration on care plans.
• Assisted in over 5000 successful births and provided post-partum counseling for struggling families to increase happiness and health of newborns and mothers.
• Trained under senior midwives for more than 20 hours to obtain qualifications.

• Company Overview: Aga khan hospital Mombasa is an acute care private facility with a 96-bed capacity. It is a premier referral hospital providing world class specialized care.
• During that period, I provided high-quality nursing care and reduced stay in time in TRIAGE from 2 hours to 30 minutes.
• Administered IV, oral, and injections of medications as directed and ensured reduction in medication errors Result: 25% drop in medical errors.
• Educated family members on patient conditions in a compassionate way.
• I assisted with conflict resolution in tense situations while being guided by ethical principles.
• I ensured that all required observations, prescribed treatment, procedures, and diagnostic tests are properly carried out in time.
• Documentation is accurately done in patients records and privacy and confidentiality highly maintained.
• There was a reduction of medication errors because of introduction of computerized documentation and tracking system.
• I maintained infection prevention by implementation of standard operating procedures and policies of policy and ensuring a safe work environment for the staff and patients in line with Joint Commission International Accreditation standards.
• I assisted consultants and Resident officers in carrying out clinical and surgical procedures.
• I promoted and maintained high standards of professional nursing care to meet the patients’ needs and increased patient satisfaction by 90% +.
• Aga khan hospital Mombasa is an acute care private facility with a 96-bed capacity. It is a premier referral hospital providing world class specialized care.

• Discussed patient care and treatment with care team members to optimize intervention plans and care delivery.
• Improved patient care by implementing evidence-based nursing practices and updating protocols.
• Provided high-quality patient education on disease prevention and management strategies, empowering patients in their own healthcare decisions.
• Managed medication administration accurately and safely, reducing the risk of adverse drug events among patients.