Senior Clinical Data Associate — Global DM Lead & SME

IQVIA LLC; Bloemfontein; On-site; ZAR 600,000 - 900,000; Full time

Job summary

IQVIA is seeking an Advanced CDA to provide timely status updates to the Data Manager and DMLs, act as the main contact for the Clinical Data Manager, and coordinate CDAs on trials with global teams.

You will proactively identify risks and mitigations and support TMF compliance reviews.Education and experience: Bachelor’s degree in Health or Science, >3 years in Data Management on clinical trials, RAVE experience, knowledge of CDISC, SDTM, and CDASH, plus strong vendor and project management

Qualifications

• Bachelor’s degree in a Health or Science discipline, with experience in clinical research.
• Advanced CDA with >3 years Data Management experience and Rave experience mandatory.
• Experience on a clinical trial in diverse, cross-functional, global teams; knowledge of CDISC, SDTM, CDASH.

Responsibilities

• Provide timely status updates to the Data Manager (DM) and DMLs; act as the main contact for the Clinical Data Manager; coordinate work of CDAs on trials with global teams; identify risks and mitigations; assist TMF compliance reviews.
• Contribute to study setup activities and data management documents (e.g., DMP, IRP); review inputs to ensure alignment with CDISC standards.

Job description

IQVIA is seeking an Advanced CDA to provide timely status updates to the Data Manager and DMLs, act as the main contact for the Clinical Data Manager, and coordinate CDAs on trials with global teams.

You will proactively identify risks and mitigations and support TMF compliance reviews.Education and experience: Bachelor’s degree in Health or Science, >3 years in Data Management on clinical trials, RAVE experience, knowledge of CDISC, SDTM, and CDASH, plus strong vendor and project management