Clinical Data Associate – Hybrid | Bloemfontein, South Africa
Location: Bloemfontein, South Africa
Job Type: Full-Time
Work Mode: Hybrid
Experience Level: 1–3 years (Base), 3+ years (Advanced)
Job Summary
IQVIA is seeking a Clinical Data Associate (CDA) to manage clinical trial data processes and documentation across multiple phases, including Study Start-up, Execution, and Close-out. Based in Bloemfontein, this hybrid role offers the opportunity to work with global teams and support data management for high-impact clinical trials using platforms like Rave EDC. Ideal candidates will have strong knowledge of data management standards such as CDISC, SDTM, and CDASH and a passion for high-quality data integrity in clinical research.
Key Responsibilities
Base Level (1–3 years):
Perform comprehensive clinical data management tasks including review, query generation, and resolution
Create eCRF completion guidelines and test data validation rules
Conduct data reconciliation across multiple data streams
Participate in study meetings, teleconferences, and close-out activities
Provide status/metric reports and manage freeze/lock of eCRFs
File documentation in the virtual Trial Master File (TMF)
Enter and manage laboratory normal ranges
Advanced Level (3+ years):
Provide proactive risk updates and status reports to Data Management (DM) and Data Management Leaders (DMLs)
Act as point of contact for Clinical Data Manager and vendor communications
Create and review Data Management documents (DVRs, IRP, DMP, eCRF guidelines)
Coordinate and delegate tasks among CDAs assigned to studies
Support TMF compliance reviews and mentor CDA staff
Serve as SME in forums and act as delegate for Data Managers
Required Skills & Qualifications
Bachelor’s degree in Health or Life Sciences
Clinical trial and data management experience (mandatory)
Rave EDC system experience (mandatory)
Strong knowledge of CDISC, SDTM, CDASH standards (for advanced level)
Proficiency in Microsoft Office tools
Strong verbal and written communication skills
Project and vendor management skills
Experience working with global, cross-functional teams
Perks & Benefits
Work on cutting-edge, global clinical research studies
Flexible hybrid work environment
Learning and development programs
Opportunity to collaborate with cross-functional and international teams
Professional growth in a highly respected clinical data environment
Company Overview
IQVIA is a world leader in healthcare intelligence, offering data, technology, and clinical research services across more than 100 countries. With an emphasis on accelerating the development of life-changing therapies, IQVIA provides innovative solutions to support pharmaceutical and healthcare organizations in improving patient outcomes.
Work Mode
Hybrid – Based in Bloemfontein, South Africa
Call to Action
Ready to shape the future of clinical data? Join IQVIA as a Clinical Data Associate and be part of a global leader in life sciences innovation.
Apply now to take your clinical data career to the next level.
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