Apply for Clinical Coding Analyst Remote Job at IQVIA with MedDRA, WHODD, SAE coding, and clinical data management experience.
IQVIA is hiring experienced professionals for the role of Clinical Coding Analyst in a remote work setup across South Africa locations including Centurion, Durban-Coastal, Bloemfontein, and Bellville.
This opportunity is ideal for candidates with expertise in clinical coding, medical dictionaries, clinical data management, and global clinical trial operations.
Candidates with experience in MedDRA, WHODD, SAE coding reconciliation, and coding quality management are encouraged to apply.
Job Details
| Particulars | Details |
|---|---|
| Company Name | IQVIA |
| Job Role | Clinical Coding Analyst |
| Work Mode | Remote |
| Employment Type | Full-Time |
| Job Requisition ID | R1538289 |
| Job Locations | Centurion, Durban-Coastal, Bloemfontein & Bellville, South Africa |
| Industry | Clinical Research / Clinical Data Management |
| Experience Required | 3 – 4 Years |
| Application Last Date | 30 June 2026 |
About the Company
IQVIA is a global leader in clinical research services, healthcare intelligence, and life sciences technology solutions. The company helps accelerate clinical development and commercialization of innovative healthcare products through advanced data-driven solutions.
Job Overview
The Clinical Coding Analyst will manage coding projects and support Clinical Data Management (CDM) activities to ensure quality data delivery within timelines and customer expectations.
The role includes medical coding, dictionary management, reconciliation activities, and collaboration with global stakeholders.
Key Responsibilities
Selected candidates will be responsible for:
- Managing standalone coding studies and coding accounts
- Performing dictionary up-versioning activities
- Conducting coding reconciliation using latest dictionary versions
- Performing external verbatim coding from non-EDC data sources
- Conducting quality control procedures for coding activities
- Managing Serious Adverse Event (SAE) coding reconciliation
- Collaborating with clients and internal stakeholders
- Identifying process improvements in coding and data management functions
- Supporting SOP and work instruction development
- Maintaining communication with CDM teams and customers
Required Skills
- Strong knowledge of MedDRA, WHODD, ICD9, and medical coding dictionaries
- Expertise in medical terminology, pharmacology, anatomy, and physiology
- Knowledge of clinical data management systems and processes
- Good understanding of global clinical drug development
- Strong project management and problem-solving skills
- Excellent English communication skills
- Ability to manage multiple global coding projects
Eligibility Criteria
Educational Qualification
Candidates with qualifications in the following fields can apply:
- Pharmacy
- Medical
- Nursing
- Dental
- Life Sciences
- Related Healthcare Fields
High School Diploma or equivalent qualification may also be considered.
Experience Required
| Experience | Requirement |
|---|---|
| Clinical Trials Experience | 3 – 4 Years |
| Coding / Data Management Experience | Required |
| Thesaurus Management Experience | Preferred |
| Global Project Handling | Preferred |
Why Join IQVIA?
Working at IQVIA offers:
- Remote working opportunity
- Exposure to global clinical research projects
- Career growth in Clinical Data Management and Coding
- Opportunity to work with international clients and teams
- Professional development and learning opportunities
How to Apply
Interested candidates can apply online through the official career portal of IQVIA before the application deadline.
Important Note
IQVIA follows a strict zero-tolerance policy regarding candidate fraud. All information provided during the recruitment process must be accurate and truthful.