Instagram
youtube
Facebook

Clinical Data Associate - Hybrid (Bloemfontein)

1-3 years
Not Disclosed
10 June 25, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc/B.Pharm/M.Pharm/Life Science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

 

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.