Clinical Supply Chain Manager: IQVIA x1
- Company: IQVIA
- Location: Bloemfontein, South Africa (Home-Office, county-wide coverage)
- Employment Type: Full-time
- Salary: R1,528,959 per annum
- Other Locations: Additional locations may be available
- Posted: 2026
Job Overview
The Clinical Supply Chain Manager is responsible for leading the end-to-end supply chain strategy for clinical trials. This role requires translating complex study protocols into efficient kit designs, robust supply plans, and seamless study execution. The role involves close collaboration with internal teams, vendors, and external partners to ensure all clinical trial materials are delivered on time and comply with the highest quality standards.
Main Purpose
To plan, manage, and oversee all aspects of clinical trial supply, including forecasting, packaging, distribution, and risk management. The role ensures clinical trial operations run smoothly while maintaining compliance with GxP, regulatory requirements, and project timelines.
Key Responsibilities
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Interpret clinical trial protocols and design effective supply chain solutions.
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Create master English label text in line with regulatory frameworks (e.g., Annex 13).
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Develop and maintain demand forecasts and packaging plans to ensure timely availability of clinical supplies.
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Initiate packaging campaigns with assigned vendors and oversee on-time delivery.
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Set up, monitor, and update study-assigned Interactive Response Technology (IRT) systems for inventory management.
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Design and oversee distribution plans executed by vendors.
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Independently manage supply to ensure materials are delivered to the right place at the right time.
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Track budgets and ensure projects adhere to client-approved quotations.
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Maintain compliance with all assigned training, GxP standards, and regulatory requirements.
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Lead client and vendor meetings to discuss supply chain status and issues.
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Create and manage Temperature Excursion plans and review associated reports.
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Conduct risk management assessments and implement appropriate mitigation strategies.
Minimum Qualifications and Experience
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Bachelor’s or higher-level degree in science or business.
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2–3 years of experience in Clinical Trials.
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At least 3 years’ experience in Clinical Supply Chain Management.
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Strong project management skills.
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Ability to establish effective working relationships with internal and external stakeholders.
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Effective communication, leadership, and problem-solving abilities.
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Proficient in Microsoft Office (Word, Excel, PowerPoint, etc.).
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Fluent in English.
Company Overview
IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence. IQVIA helps accelerate the development and commercialization of innovative medical treatments to improve patient outcomes and population health worldwide.
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Committed to hiring integrity and maintains zero tolerance for candidate fraud.