Senior Clinical Data Associate: Drive Data Management Impact

IQVIA; Centurion; On-site; ZAR 700,000 - 1,100,000; Full time

Job summary

IQVIA is seeking a Senior CDA to lead data management activities on global clinical trials from our Centurion office. You will coordinate CDA work, mentor staff and collaborate with the Global Data Management team to ensure TMF compliance and timely study deliverables.

The role requires a Bachelor’s degree in health or science, more than three years of CDA/Data Management experience, Rave expertise, and strong knowledge of CDISC SDTM/CDASH.

Qualifications

• Bachelor’s degree in health or science with clinical research experience.
• Advanced CDA: 3+ years of data management experience.
• Data management on a clinical trial is mandatory.
• Rave experience mandatory.
• Experience in diverse, cross-functional, global teams.
• Knowledge of CDISC SDTM/CDASH for Advanced CDA.
• Knowledge of platforms to capture and process data.
• Strong project and vendor management skills.
• Proficiency with Microsoft Office tools.

Responsibilities

• Provide timely status updates including issues & risks to DM and DMLs as needed
• Act as the Point of contact for Clinical Data Manager, pro-active to identify risks and mitigations
• May communicate with vendors to resolve reconciliation issues
• Provide input to Study set up activities including DVR creation
• Create and/or provide inputs to Data Management documents (eCRF completion guidelines, etc.)
• Review and provide inputs to Data Management documents (IRP, DMP, etc.)
• Assign work to allocated CDAs on a trial; coordinate with Global DM on priorities
• Assist the Data Management Leader in TMF compliance reviews
• Train and mentor CDA staff; may serve as SME

Skills

CDA advanced level

Rave experience

CDISC standards

SDTM/CDASH knowledge

Project management

Vendor management

MS Office proficiency

Education

Bachelor’s degree in Health or Science

Tools

Rave

Job description

IQVIA is seeking a Senior CDA to lead data management activities on global clinical trials from our Centurion office. You will coordinate CDA work, mentor staff and collaborate with the Global Data Management team to ensure TMF compliance and timely study deliverables.

The role requires a Bachelor’s degree in health or science, more than three years of CDA/Data Management experience, Rave expertise, and strong knowledge of CDISC SDTM/CDASH.