Jemima Jesse

Conduct detailed patient assessments and develop individualised treatment plans for

outpatient and inpatient care

 Diagnose and manage a wide range of medical conditions with minimal supervision

 Prescribe, review, and adjust medications in line with evidence-based and facility

protocols

 Perform minor surgical and outpatient procedures (suturing, wound care, incision &

drainage)

 Provide emergency and acute care, including triage, stabilisation, and timely referrals

 Order and interpret laboratory, radiology, and diagnostic tests to guide management

 Manage chronic conditions (e.g., hypertension, diabetes, asthma) with structured follow￾up plans

 Deliver maternal, reproductive, and child health services, including antenatal and family

planning care

 Ensure accurate, timely documentation in EMR systems and maintain high-quality

patient records

 Deliver high standards of patient-centered care to enhance satisfaction and retention in a

private setting

 Coordinate care with consultants, nurses, and specialists to optimise patient outcomes

 Participate in clinical audits, quality improvement initiatives, and adherence to hospital

standards

 Enforce infection prevention and control (IPC) protocols and patient safety measures

 Manage referrals and ensure proper follow-up for continuity of care

• Recruited, enrolled, and obtained consent from participants
• Ensured signed informed consents are returned, filed in the ISF, and kept under a locked cabinet after each data collection day
• Implemented quality policies, SOPs, and monitoring tools
• Prepared study sites for data storage and transfer
• Ensured that direct access to source data/documents is available for study-related monitoring, audits, IRB review, and sponsor requests
• Maintained and controlled all study records and documentation, including CRFs, information, and consent forms, and provided copies to the sponsor as requested
• Disseminated protocol/amendments to sites
• Reported project performance against established standards
• Participated in internal audits, monitoring visits, training activities, and inspections
• Contributed to the preparation and submission of reports as needed
• Maintained effective stock control for study supplies and consumables
• Ordered study supplies and consumables
• Complied with all health and safety guidelines
• Collaborated with the principal investigator, co-investigators, and other team members to gather requirements for manual or electronic data capture systems
• Provided timely responses to the research team, monitoring team, and database administrators to resolve queries quickly
• Ensured compliance with protocol, SOPs, guidelines, and good practices

• Triaged and established healthcare needs for clients in the Comprehensive Care Clinic.
• Provided HIV care to adults, adolescents, and children based on MOH guidelines and recommendations.
• Monitored the HIV-positive client by conducting routine blood sample collection for viral load
• Provided information and counseling to clients on prevention and adherence to medication
• Spearheaded the provision of reproductive health services, which include family planning and cervical cancer screening.
• Utilized EMR systems for data collection and patient information management, ensuring accuracy and confidentiality.
• Provided TB care and intervention to all affected persons.
• Assisted in coordinating community follow-up of patients initiated on treatment.
• [Murang'a County]

• Assisted in conducting clinical research studies, focusing on pneumonia in children between 2-59 months.
• Managed patient screening, recruitment, consent, and follow-up for research participants.
• Coordinated with research teams to ensure study protocols and ethical guidelines were adhered to.
• Utilized the RedCap system for data collection and patient information management, ensuring accuracy and confidentiality.
• Worked with hospital staff to ensure appropriate administration of the study intervention to enrolled participants.
• Managed and recorded incidental illnesses and any side effects from the study investigational product.
• Recorded and reported any severe adverse events observed or reported by the caregiver immediately within 24 hours to the scientific and ethics review unit.
• Presented weekly reports of clinic activities on patients enrolled and all excluded and reasons for exclusion.
• Facilitated both internal and external study monitoring visits.
• Managed stock inventory for trial drugs and other consumable supplies within the study site.
• Promptly addressed data queries.
• Maintained the trial master file.
• Participated in Pre-study site induction and close-out.
• Conducted research as per the standard operating procedures(SOPs), study protocol, Clinical Quality Management Plan(CQMP), and the Kenya Paediatric guideline provided.
• Conducted quarterly training for new members of staff
• Thika Level 5 Hospital station

• Conducted comprehensive patient assessments, diagnosed medical conditions, and developed appropriate treatment plans.
• Administered treatments, performed minor surgical procedures, and managed patient follow-ups to ensure optimal health outcomes.
• Managed patients in COVID-19 isolation unit.
• Educated patients and families on disease prevention, health maintenance, and treatment plans.
• Collaborated with multidisciplinary teams to provide coordinated and holistic patient care.
• Assisted in designing and conducting clinical research studies, focusing on [specific area of research].
• Collected, analyzed, and interpreted research data, contributing to developing scientific publications and presentations.
• Managed patient recruitment, consent, and follow-up for research participation.
• Coordinated with research teams to ensure study protocols and ethical guidelines adherence.
• Utilized EMR systems for data collection and patient information management, ensuring accuracy and confidentiality.