IQVIA Jobs in South Africa

We are looking for data management expert who has prior experience in performing scientific (complex) clinical data review in close collaboration with the Study Responsible Physicians (SRP) and Study Responsible Scientists (SRS) · ...

This is your opportunity to work cross‑functionally on complex, high‑impact programs that help shape the future of healthcare. · Lead and coordinate adjudication and oversight committees across CEVA service lines · Serve as the primary customer interface, ensuring strong communic ...

We are recruiting for Site Activation Coordinators to support country-level activities that enable clinical trial sites to begin operations. · As a Site Activation Coordinator, you will collaborate with cross-functional teams, manage study documentation, ensure compliance and hel ...

The Clinical Data Specialist will provide basic and some comprehensive data management expertise to the Clinical Data Management team. · Serve as a Data Operations Coordinator for one protocol · May lead database audit team · May develop and test databases · ...

The Data Team Lead manages end-to-end delivery of data management services for single/multi-service projects with minimal guidance. · Ensure quality deliverables on time and within budget to customer satisfaction. · ...

The Financial Accountant at IQVIA plays a key role in delivering accurate and timely financial reporting, ensuring full compliance with statutory and internal requirements, and supporting informed business decision-making through detailed financial analysis. This role supports co ...

Join us in driving excellence across global clinical research programs. Are you a proactive leader with deep clinical research expertise and a passion for delivering high-quality outcomes for customers? We're looking for a Sr CEVA Specialist to provide strategic oversight and ope ...

We are looking for a Sr CEVA Specialist to provide strategic oversight and operational excellence across Endpoint Adjudication Management (EAM) and Oversight Group Management (OGM) projects. This is your opportunity to work cross-functionally on complex, high-impact programs that ...

Project Leads are an integral part of clinical trial delivery, liaising with clinical teams to improve patients' lives by bringing new drugs to the market faster. · ...

We are seeking a detail‑oriented and proactive Centralized Monitoring Assistant to provide essential administrative and operational support to our clinical study management teams. · ...

You'll be responsible for managing end-to-end delivery of data management services for multi-service projects ensuring quality deliverables on time and within budget. · ...

IQVIA Biotech está buscando un Especialista en Viabilidad de Sitios Senior para apoyar su equipo de operaciones clínicas creciente. · ...

We're recruiting for both Entry-Level and Senior Site Activation Coordinator positions. · Your level will be determined based on your experience, capability, and career trajectory. · Support feasibility assessments. · Work closely with Site Activation Managers. · ...

Job Overview · Direct and manage the delivery of all required site activation, maintenance and regulatory activities for selected studies or multi-protocol programs, including pre-award activities, oversight of the scope of work, budget and resources. · Essential Functions · Over ...

Manage end-to-end delivery of data management services for single/multi-service projects with minimal guidance ensuring quality deliverables on time and within budget to customer satisfaction. · ...

Join our Global Site Activation Team and drive high-quality site activation to ensure patients gain access to safe and effective treatments. · ...

We are looking for a proactive leader with deep clinical research expertise to provide strategic oversight and operational excellence across Endpoint Adjudication Management (EAM) and Oversight Group Management (OGM) projects. · Manage And Deliver Comprehensive Clinical Event Val ...

Job Summary · We are seeking a highly skilled Data Acquisition Expert (eSource Specialist) to join our team. The ideal candidate will be responsible for acquiring Electronic Health Record (EHR) and integrating it with Electronic Data Capture (EDC) system to automate data entry pr ...

Job Advert: Study Coordinator (Limited Duration Contract) – Cape Town · Location: Cape Town, South Africa · Contract Type: Limited Duration Contract (LDC) · Seniority Level: Mid to Senior · Start Date: As soon as possible · About the Role · We are seeking an experienced Study Coo ...

Join our Global Site Activation Team, a 2,000-strong network driving high-quality site activation and ensuring patients gain access to safe and effective treatments. · Lead and support ICF development (master & country level) · ...