Clinical Data Associate - Base

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

Job summary

A leading global provider of clinical research services is seeking a Base Level Data Manager in Bloemfontein, South Africa. The role involves comprehensive data management tasks, report generation, and data reconciliation for clinical trials. Candidates should possess a Bachelor's degree in a Health or Science discipline, have 1-3 years of data management experience and be familiar with Rave. This position offers an opportunity to work within a diverse team and contribute to innovative medical treatments.

Qualifications

• Bachelor’s degree in a Health or Science discipline with experience in clinical research.
• 1-3 years of experience in Data Management at a CRO/Pharma.
• Rave experience mandatory.

Responsibilities

• Perform comprehensive data management tasks including data review.
• Create and provide status/metric reports.
• Manage Freeze / lock of eCRF.

Skills

Data Management experience

Project management skills

Vendor management skills

Proficiency with Microsoft Office tools

Knowledge of current industry standards

Experience working in diverse teams

Rave experience

Education

Bachelor’s degree in a Health or Science discipline

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