kelemogile - DATA CAPTURER RESEARCH STUDY ASSISTANT

Demonstrated experience with Clinical Data Management.

Demonstrated experience with Data Validation & Quality Assurance.

Demonstrated experience with Data Cleaning & Data Integrity.

Demonstrated experience with Clinical Research Support.

Demonstrated experience with Participant Recruitment & Retention.

I recruited eligible pregnant women into clinical research studies by conducting participant outreach, assessing eligibility against study inclusion and exclusion criteria, and explaining study objectives.. I facilitated the informed consent process by clearly explaining study procedures, participant rights, potential risks, and benefits before obtaining signed Informed Consent Forms (ICFs).. I conducted pre-screening interviews by collecting demographic and clinical information, verifying participant eligibility, and documenting findings accurately.. I captured, verified, and maintained participant and clinical research data by accurately recording information in study databases, logs, registers, and case report forms while validating data against source documents.. I identified and resolved data discrepancies, missing information, and inconsistencies by reviewing study records, liaising with clinicians and research staff, and updating records accordingly.. I scheduled participant appointments and coordinated follow-up visits by maintaining appointment schedules, communicating with participants, and sending reminders to minimise missed visits and improve participant retention throughout the study.

I captured and maintained accurate patient information by receiving clinical records from healthcare professionals, verifying supporting documentation, and recording patient data on Tier.Net, ETR.Net, and DHIS.. I reviewed patient records for completeness by identifying missing information, inconsistencies, and data entry errors before following up with clinicians and programme managers to obtain accurate information.. I verified captured information against source documents by performing routine quality checks, correcting discrepancies, and updating patient records where necessary.. I captured confidential patient information relating to HIV and TB programmes while maintaining strict confidentiality and ensuring compliance with organisational policies, ethical standards, and data protection requirements.. I maintained Clinical ART and TB stationery by updating patient records, ensuring documentation was complete, and supporting clinicians with accurate clinical information.. I captured and maintained Case Identification Registers on ETR.Net by recording patient information accurately, updating records promptly, and ensuring compliance with programme reporting requirements.

I captured and maintained accurate patient information by recording HIV and TB patient data on Tier.Net, ETR.Net, and DHIS while verifying source documents for completeness and accuracy.. I maintained accurate administrative records by organising project documentation, contracts, invoices, purchase orders, delivery notes, and correspondence to ensure effective document control and compliance with company procedures.. I prepared and processed project documentation, including quotations, invoices, purchase orders, and supplier requests, ensuring all records were accurate, complete, and submitted within required timeframes.. I monitored project correspondence by tracking incoming and outgoing communications, following up on outstanding actions, and ensuring stakeholders remained informed of project developments.. I followed up on outstanding customer payments by communicating with clients, maintaining payment records, and coordinating with the finance team to ensure timely collections.