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Clinical Data Specialist - Hybrid - Bloemfontein

1-3 years
Not Disclosed
10 June 25, 2025
Job Description
Job Type: Hybrid 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 Specialist – Hybrid – Bloemfontein, South Africa

Location: Bloemfontein, South Africa
Experience Required: 1–3+ years (Base or Advanced CDA level)
Work Mode: Hybrid
Job Type: Full-Time
Company: IQVIA


Job Summary

IQVIA, a global leader in clinical research and healthcare data solutions, is hiring a Clinical Data Specialist for its hybrid team in Bloemfontein, South Africa. This is a key role supporting global clinical trials through efficient data review, reconciliation, and data management processes across the entire study lifecycle—from start-up to closeout. The position is ideal for professionals with at least 1 year of experience in clinical data management, looking to grow within a fast-paced, global healthcare environment.


Key Responsibilities

  • Perform comprehensive data review, query generation, and resolution

  • Reconcile clinical data streams and track EDC data cleaning progress

  • Participate in study meetings and teleconferences

  • Manage freeze/lock processes of eCRFs and maintain Trial Master File documentation

  • Conduct study close-out and CRF archival QC

  • Provide input to Data Management Plans (DMPs) and related documentation

  • Train and mentor Clinical Data Associates (CDAs)

  • Collaborate with Global Data Managers (GDMs) and vendors on data issues

  • Support testing of data validation rules and eCRF completion guidelines

  • Generate status and metric reports and provide regular updates to study leadership


Required Skills & Qualifications

  • Bachelor's degree in Health, Science, or related discipline

  • 1–3+ years of experience in clinical data management (CDA Base or Advanced level)

  • Strong understanding of clinical trial lifecycle and data workflows

  • Familiarity with CDISC, SDTM, CDASH, and other industry data standards

  • Hands-on experience with EDC systems and Microsoft Office tools

  • Strong written and verbal communication skills

  • Experience working in global, cross-functional clinical teams

  • Ability to interpret and present clinical trial data trends

  • Project management and vendor coordination experience preferred


Perks & Benefits

  • Hybrid work flexibility in Bloemfontein

  • Competitive salary (not explicitly mentioned; based on experience)

  • Career advancement opportunities within a global CRO

  • Exposure to global clinical trials and data systems

  • Professional training and mentoring programs

  • Collaborative and diverse team culture


Company Overview

IQVIA is a top global provider of clinical research services, real-world data insights, and healthcare intelligence. Operating in 100+ countries, IQVIA partners with the life sciences industry to accelerate the development and commercialization of life-saving treatments.


Work Mode

Hybrid – Bloemfontein, South Africa


Call to Action

Ready to take your clinical data career to the next level? Join IQVIA as a Clinical Data Specialist and contribute to global trials that make a difference.
Apply now and be part of a transformative journey in healthcare research.