Overview
Clinical Data Specialist – Hybrid – Bloemfontein Jobs in Bloemfontein, Free State, South Africa at IQVIA
Title: Clinical Data Specialist – Hybrid – Bloemfontein
Company: IQVIA
Location: Bloemfontein, Free State, South Africa
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
ADVANCED
Provide timely status updates including issues & risks to GDM and DMLs as needed
Act as the Point of contact for Global Data Manager/Clinical Data Manager, working pro-actively to identify risks and provide mitigations
May communicate with the vendors to resolve reconciliation issues.
Provide input to Study set up activities including but not limited to creation of DVRs
Create and/or provide inputs to Data Management documents (e.g. eCRF completion guidelines, etc.).
Review and provide inputs to Data Management documents (e.g. IRP, DMP, etc.)
Assign work to allocated CDAs on a trial. Coordinate work of CDAs assigned to a study working closely with the Global Data Manager to understand priorities and timelines.
Assist the Data Management Leader in TMF compliance reviews.
Train and mentor CDA staff
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.
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 tool
Highly organized with excellent written and verbal communication.
Ability to interpret clinical trial data and present trends to clinical trial team on data.
Experience CDA BASE level: 1-3 years of experience.
Experience CDA ADVANCED level: >3 year of experience
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