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IQVIA’s Global Site Activation team is seeking a Maintenance Associate to support study delivery during the maintenance phase. You will work with Maintenance Leads and CTRMs to ensure maintenance and regulatory activities are completed accurately across studies.
Responsibilities include maintaining systems, tracking tools, timelines, and budgets, while collaborating with stakeholders to ensure compliance and timely execution across time zones and geographies.
Centurion, South Africa
Belgrade, Serbia
Lisbon, Portugal
Budapest, Hungary
Kyiv, Ukraine
Zagreb, Croatia
Prague, Czech Republic
Sofia, Bulgaria
Madrid, Spain
Bucuresti, Romania
Full time
R1538197
Make an impact on patient health!
IQVIA’s Global Site Activation Team of 2000 employees, drives best in class site and customer experience, with industry leading outcomes. We keep the patient at the forefront; ‘Always Impatient for the Patient’ and we excel in our collaboration with our external/internal customers. IQVIA’s Country Site Activation team are a global network who identify and activate sites to the highest quality to ensure patients on Clinical trials have access to safe and effective medication. We are leaders in innovation and first to new technologies, meaning a vast amount of career development opportunities are available.
As a Maintenance Associate , you will play a key role in supporting study delivery during the maintenance phase of clinical studies. Working closely with Maintenance Leads and Clinical Trial & Relationship Managers (CTRMs), you will help ensure the successful completion of all required maintenance and regulatory activities across assigned studies or multi‑protocol programs.
You will be responsible for understanding the scope of work, budgets, and resource requirements, and for ensuring study activities are executed accurately and efficiently.
Support the setup, updating, and ongoing maintenance of internal systems, databases, tracking tools, timelines, and project plans with complete and accurate study‑specific information.
Collaborate with cross‑functional stakeholders to ensure maintenance and regulatory activities are completed in line with timelines, budgets, and compliance requirements.
Manage, utilize, and interpret various study dashboards to analyze data, monitor study metrics, and track compliance.
Proactively identify risks, issues, and trends through data analysis and escalte appropriately.
Bachelor’s Degree in Life Science or related field
Minimum 3 years’ work experience; preferably in in healthcare or similar
Good knowledge of MS Office
Fluent in English
Good interpersonal, communication and organizational skills to establish and maintain effective working relationships with co-workers, managers and sponsors
Ability to work on multiple projects
Ability to work across time-zones, cultures and geographies
Exposure across 21 Therapeutic Areas
Be part of a global team who operate across 141 locations
Exposure across a variety of studies and projects
Access to new, innovative technologies
Work within a collaborative and vibrant environment
Own your career!
It takes passion to make the extraordinary possible for patients. Our culture of innovation and collaboration enables us to explore new possibilities and help improve health around the world. When you join our diverse, global team, you’ll harness the power of unparalleled data, advanced analytics, cutting‑edge technologies, and deep healthcare and scientific expertise to drive healthcare forward.
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.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
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