Key Responsibilities

• Manage incoming clinical research data across multiple worksheets, systems, and image files.
• Ensure accurate data entry and escalate issues appropriately.
• Apply critical thinking and discretion, particularly in relation to adverse events.
• Upload visit data within defined timelines.
• Review project data and deliver results to stakeholders promptly.
• Request and manage source data corrections as required.
• Enter/upload data into third-party platforms (e.g., EDC systems).
• Review and resolve data queries.
• Participate in database lock activities.
• Conduct regular quality checks of data for completeness, accuracy, and integrity (ALCOA+).
• Assist in the identification and reporting of potential adverse events.
• Maintain project documentation and the Trial Master File (TMF).
• Assist in the creation and maintenance of case report forms.

Qualifications:

• Matric certificate (minimum requirement).
• Bachelor’s degree in a life sciences-related field (Advantagouss).
• 1–2 years of clinical trial and data management experience.
• Knowledge of Good Clinical Practices (GCP).
• Experience with electronic data capture (EDC) systems (preferred).
• Strong skills in the use of technology, tools, operating systems, and software.
• Strong organizational skills with experience balancing priorities and resources.
• Strong attention to detail.
• Critical thinking and problem-solving skills.
• Ability to plan proactively, anticipate challenges, and operationalize solutions.
• Able to work thoughtfully and decisively, fostering an inclusive work environment.
• Clear criminal record.
• Clear credit record.