Location: South Africa / Kenya
Business Unit: IQVIA – Real World Evidence
Reporting to: Associate Principal
Role Overview
The Study Manager is responsible for the operational planning, coordination, and delivery of Real World Evidence (RWE), observational, and global health projects across Sub‑Saharan Africa region. The role focuses on hands‑on project execution, ensuring projects are delivered on time, within scope, budget, and quality expectations, in compliance with IQVIA SOPs, local regulatory requirements, and client commitments.
This role plays a critical part in enabling in‑country and multi‑country RWE delivery, working closely with local country teams, investigator sites, ethics committees, and global IQVIA functions. The Study Manager supports projects that often involve non‑traditional study designs, heterogeneous data sources, variable infrastructure, and country‑specific regulatory and operational constraints, requiring strong coordination and problem‑solving skills.
The role operates under the guidance of senior project leadership and may manage multiple projects or workstreams simultaneously.
Key Responsibilities
Project Planning & Delivery
Support end‑to‑end delivery of RWE, observational, registry, retrospective, and prospective studies across Africa
Translate project plans into actionable timelines, milestones, and deliverables
Coordinate start‑up, execution, monitoring, and close‑out activities
Track project progress against plan and proactively manage deviations
Maintain accurate project documentation, trackers, and study records
Cross‑Functional & Country Coordination
Coordinate internal cross‑functional teams (e.g. clinical operations, data management, regulatory, epidemiology, biostatistics)
Work closely with local country teams to ensure feasibility, site readiness, and operational alignment
Support coordination with investigator sites, and third‑party vendors
Facilitate internal and external project meetings and document actions and decisions
Stakeholder & Client Support
Act as a day‑to‑day operational contact for assigned projects or workstreams
Support client communications, including routine status updates, progress reports, and meeting preparation
Escalate risks, issues, and changes appropriately to senior project leadership
Support relationship management by ensuring reliable, transparent delivery
Risk, Quality & Compliance
Identify project risks and issues, including country‑specific operational and regulatory risks
Support development and tracking of mitigation actions
Ensure compliance with IQVIA SOPs, quality standards, and applicable local regulations (e.g. ethics approvals, data protection requirements)
Support audit readiness and inspection preparedness activities when required
Financial & Resource Support
Support tracking of project budgets, forecasts, and resource utilization for assigned scope
Assist in monitoring financial performance and cost drivers
Support vendor oversight activities, including tracking deliverables and timelines
Africa‑Specific Context
Support delivery in resource‑variable settings, including sites with differing infrastructure and experience levels
Navigate country‑specific regulatory, ethics, and contracting processes
Support studies that require on‑the‑ground coordination, site engagement, and local troubleshooting
Contribute to scalable and sustainable RWE delivery models across multiple African countries
Required Qualifications & Experience
Bachelor’s degree in life sciences, pharmacy, epidemiology, or a related field
At least 1 year of experience in project coordination or project management within healthcare, clinical research, RWE, or public health
Experience working with cross‑functional, matrixed teams
Exposure to RWE, observational studies, registries, or public health projects is an advantage
Experience working in South Africa and/or Sub‑Saharan Africa strongly preferred
Locations: South Africa and Kenia
Key Skills & Competencies
Strong organizational and planning skills
Ability to manage multiple priorities and deadlines
Clear and professional written and verbal communication
Proactive problem‑solving and risk awareness
Stakeholder management and collaboration skills
Attention to detail and commitment to quality
Comfort working in complex, fast‑paced d
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
What We Do
IQVIA (NYSE:IQV) is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. IQVIA creates intelligent connections across all aspects of healthcare through its analytics, transformative technology, big data resources and extensive domain expertise. IQVIA Connected Intelligence™ delivers powerful insights with speed and agility — enabling customers to accelerate the clinical development and commercialization of innovative medical treatments that improve healthcare outcomes for patients. With approximately 70,000 employees, IQVIA conducts operations in more than 100 countries. To learn more, visit www.iqvia.com.







