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Salary
$30k – $78k per year (Estimated)
Location
In office (Sofia, Belgrade, Lisbon, Budapest, Tallinn, Zagreb, Athens, Centurion, Prague, Ljubljana, Madrid, Romania)
Seniority
Staff
Employment
Full-Time
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IQVIA is an American company formed in 2016 by the merger of the contract research organisation Quintiles, founded in 1982, with the pharmaceutical data business IMS Health. It runs clinical trials on behalf of drug and device makers and simultaneously operates one of the largest healthcare data estates in the world, covering prescriptions, claims and electronic medical records, which it sells back to the same industry for commercial planning and real-world evidence studies. Headquartered in Durham, North Carolina and listed on the New York Stock Exchange, it employs close to ninety thousand people and combines the trial and data businesses in what it calls connected intelligence.

At IQVIA, our Clinical Leads play a vital role in bringing innovative medicines to patients worldwide. You'll provide clinical leadership across regional and global clinical trials, partnering with Project Leaders, sponsors and cross-functional teams to ensure studies are delivered with a focus on quality, patient recruitment, site performance and operational excellence.

This is an exciting opportunity to lead the clinical delivery of complex studies while expanding your expertise in study execution, stakeholder management and clinical operations within one of the world's leading clinical research organizations.

Why Join Global Study Leadership?

Global Study Leadership is a global, full-service team delivering clinical trials through both therapeutically aligned and customer-dedicated delivery models. You'll work across a diverse portfolio including Oncology, Rare Disease, CNS, Cardiovascular, Immunology, Respiratory, Cell & Gene Therapy, Infectious Disease, Ophthalmology and Women's Health while partnering with leading pharmaceutical and biotechnology sponsors around the world.

Working alongside experienced project leaders and clinical operations experts, you'll have the opportunity to broaden your therapeutic expertise, strengthen your leadership capabilities and influence the successful delivery of studies that help bring new treatments to patients faster. Supported by a collaborative global network, mentorship, flexible ways of working and AI-enabled technology and data-driven insights, you'll be empowered to grow your career while making a meaningful impact on global healthcare.

What You'll Be Doing

As a Clinical Lead, you'll be accountable for the clinical delivery of assigned studies, ensuring recruitment, site performance, quality and operational objectives are achieved while maintaining compliance with regulatory requirements and customer expectations.

Key Responsibilities

  • Lead the clinical delivery of regional and global clinical studies, ensuring projects meet quality, timeline, recruitment and operational objectives

  • Drive patient recruitment and site engagement strategies, ensuring enrolment targets are achieved and studies remain on track

  • Partner with Project Leaders and cross-functional teams to drive study milestones, resolve issues and maintain operational excellence

  • Provide leadership and guidance to clinical teams, supporting resource planning, training and project delivery

  • Manage clinical risks, oversee quality standards and drive proactive mitigation strategies throughout the study lifecycle

  • Build strong relationships with internal and external stakeholders, ensuring effective communication and alignment across study teams

  • Support financial oversight of clinical delivery, including forecasting, budget management and identification of scope changes where applicable

  • Contribute to continuous improvement initiatives, knowledge sharing and the development of less experienced team members

  • Support proposal development, bid defence activities and clinical delivery planning for new opportunities where appropriate

What We're Looking For

  • Bachelor's degree in Life Sciences, Healthcare, or a related scientific discipline

  • 5+ years of clinical research, monitoring, or clinical operations experience within a CRO, pharmaceutical, or biotechnology environment

  • Strong understanding of clinical trial conduct, ICH-GCP guidelines and applicable regulatory requirements

  • Experience leading clinical study delivery activities, including patient recruitment, site management and clinical quality oversight

  • Proven ability to collaborate across cross-functional teams and manage internal and external stakeholders in a global environment

  • Strong communication, problem-solving, organizational and decision-making skills

  • Experience supporting project financial management and operational planning is desirable

  • Passion for advancing clinical research and improving outcomes for patients worldwide

Build Your Future with IQVIA

If you're looking for a role that combines clinical leadership, global study exposure, cross-functional collaboration and career growth, we'd love to hear from you. At IQVIA, you'll have the opportunity to work on high-profile clinical trials, collaborate with industry-leading sponsors, leverage innovative technology and build a rewarding career within a global organization dedicated to transforming healthcare and improving patient outcomes around the world.

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.

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