Clinical Data Associate - Base

IQVIA; Centurion; On-site; ZAR 200 000 - 300 000; Full time

Job summary

A leading global provider of clinical research services is seeking a Data Management professional in Centurion, South Africa. The role includes managing comprehensive data management tasks, ensuring data accuracy, and contributing to study-related activities. Candidates should have a Bachelor's degree in Health or Science, 1-3 years of experience in data management, and proficiency in Rave. This position offers insights into clinical research processes and opportunities for career growth.

Qualifications

• Experience in clinical research and data management is mandatory.
• 1-3 years of experience in Data Management at a CRO/Pharma required.
• Knowledge of industry standards like CDISC, SDTM, and CDASH.

Responsibilities

• Perform comprehensive data management tasks including data review and query resolution.
• Conduct ongoing Data Reconciliation of all data streams.
• Create and provide status/metric reports.

Skills

Data Management

Project management

Vendor management

Proficiency with Microsoft Office tools

Education

Bachelor’s degree in Health or Science discipline

Tools

Rave

Job description

Base level role

• Perform comprehensive data management tasks including data review, query generation and query resolution. This may also include, but is not limited to creation of eCRF completion guidelines, entry of test data for eCRF and the Data Review Model, testing of data validation rules, etc. Data Management tasks should be inclusive of 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

Education and Experience Guidelines

• Bachelor’s degree in a Health or Science discipline with experience in clinical research.
• Data Management experience and experience working on a clinical trial mandatory.
• Rave experience mandatory
• Experience working in highly diverse teams within clinical research; cross-functional, global, multi- regional.
• Knowledge of current industry standards (e.g., CDISC, SDTM, CDASH, etc.) for Advanced CDA.
• Knowledge of technology 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 of experience in Data Management at a CRO/Pharma

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide . Learn more at https://jobs.iqvia.com