Clinical Data Associate — Rave/EDC Data Management

IQVIA; Centurion; On-site; ZAR 1,384,000 - 1,692,000; Full time

Job summary

IQVIA is seeking a base level Data Management professional in South Africa to support clinical trials from study start to close-out. You will perform data review, query resolution, data reconciliation, and maintain eCRF lifecycle within a global, cross-functional team.

The role requires a Bachelor’s in health/science, 1–3 years in data management at a CRO/Pharma, and Rave experience. You’ll collaborate across regions, apply CDISC standards, and manage TMF documentation, with opportunities to

Qualifications

• Bachelor’s degree in health or science with clinical research experience.
• Data Management experience in a clinical trial mandatory.
• Rave experience mandatory.
• Experience in diverse, cross-functional, global teams.
• Knowledge of CDISC SDTM CDASH for Advanced CDA.
• Knowledge of technology platforms to capture and process data.
• Project management and vendor management skills.
• Proficiency with Microsoft Office tools.
• CDA BASE level: 1-3 years of Data Management at a CRO/Pharma.

Responsibilities

• Perform comprehensive data management tasks including data review, query generation and resolution across study phases.
• Perform ongoing data reconciliation of all data streams.
• Attend study related meetings/teleconferences.
• Perform study closeout/archiving activities including QC of archival CRFs.
• Create and provide status/metric reports.
• Generate reports on EDC and track cleaning progress.
• Manage freeze/lock of eCRF.
• File documentation in the virtual Trial Master File (TMF).
• Receives and enters lab normal ranges.

Skills

Data management

Clinical research

Rave experience

CDISC knowledge

Project management

Vendor management

MS Office

Team collaboration

Education

Bachelor’s degree in Health or Science

Tools

Rave

TMF management tools

MS Office

Job description

IQVIA is seeking a base level Data Management professional in South Africa to support clinical trials from study start to close-out. You will perform data review, query resolution, data reconciliation, and maintain eCRF lifecycle within a global, cross-functional team.

The role requires a Bachelor’s in health/science, 1–3 years in data management at a CRO/Pharma, and Rave experience. You’ll collaborate across regions, apply CDISC standards, and manage TMF documentation, with opportunities to