Clinical Data Specialist — Rave & Trial Data Management

IQVIA; Bloemfontein; On-site; ZAR 360,000 - 540,000; Full time

Job summary

IQVIA is a leading global provider of clinical research services, with a focus on data management for clinical trials. The role involves comprehensive data management tasks across study start-up, execution and close-out, including data review, reconciliation and query resolution, in a global, cross-functional setting.

We seek candidates with a health/science degree, 1–3 years of data management experience at CRO/Pharma, and mandatory Rave experience.

Qualifications

• Bachelor's degree in Health or Science with experience in clinical research.
• Data Management experience and experience working on a clinical trial mandatory.
• Rave experience mandatory.
• Experience working in diverse, cross-functional, global teams.
• Knowledge of industry standards (CDISC, SDTM, CDASH) for Advanced CDA.
• Knowledge of platforms and systems to capture and process data.
• Project management skills.
• Vendor management skills.
• Proficiency with Microsoft Office tools.
• Experience CDA BASE level: 1–3 years in Data Management at a CRO/Pharma.

Responsibilities

• Perform comprehensive data management tasks including data review, query generation and query resolution.
• Data Management tasks should include Study Start-up, Execution, Database Lock and Close-out.
• Perform ongoing Data Reconciliation of all data streams.
• Attend study related meetings/teleconferences.
• Perform Study Closeout/Archiving Activities including QC of subject/site 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

Query resolution

Data review

Cross-functional teamwork

Project management

Vendor management

MS Office

Education

Bachelor's degree in Health or Science

Tools

Rave

Microsoft Office

Job description

IQVIA is a leading global provider of clinical research services, with a focus on data management for clinical trials. The role involves comprehensive data management tasks across study start-up, execution and close-out, including data review, reconciliation and query resolution, in a global, cross-functional setting.

We seek candidates with a health/science degree, 1–3 years of data management experience at CRO/Pharma, and mandatory Rave experience.