Key Responsibilities:
- Accurately enter participant information and
clinical/research data into electronic systems such as ODK, OpenMRS, and
REDCap.
- Maintain organized participant files, source
documents, CRFs, and results in compliance with study protocols.
- Conduct routine data cleaning, validation, and
discrepancy resolution to ensure data quality and integrity.
- Perform regular data backups and ensure secure
storage of all study records.
- Cross-check data against source documents and
prepare materials for monitoring visits and audits.
- Generate routine data summaries, tracking logs,
and progress reports to support study operations.
- Collaborate with clinical and field teams to
reconcile data and provide updates during study meetings.
- Provide general data-related support as assigned
to ensure smooth and timely study
Vacancy Requirements:
- Diploma in Health Records and Information or
equivalent training. Mandatory
- Previous experience in data entry or records
management in a healthcare or research setting preferred. Mandatory
- Basic computer literacy and proficiency in
Microsoft Office (Word, Excel) and data entry platforms (ODK, OpenMRS,
Redcap). Mandatory
- Ability to maintain confidentiality of
participant information. Good communication and teamwork skills Mandatory
How to Apply
