Global Study Leadership - Clinical Lead - MASH

IQVIA; Madrid; Presencial; EUR 85.000 - 115.000; Jornada completa

Descripción de la vacante

IQVIA is seeking a Clinical Lead to oversee the clinical delivery of regional and global studies, ensuring recruitment, site performance, quality and regulatory compliance. You will work with cross-functional teams and senior project leaders to meet timelines and operational objectives.

The role offers exposure to oncology, rare disease, CNS, and other therapeutic areas, with opportunities to mentor others and influence study success across a global network.

Formación

• 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.

Responsabilidades

• 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

Conocimientos

Clinical research experience

Study delivery leadership

Cross-functional collaboration

Communication & problem-solving

Financial & budgeting support

Educación

Bachelor's degree in Life Sciences, Healthcare, or related

Descripción del empleo

Sofia, Bulgaria

Madrid, Spain

Belgrade, Serbia

Lisbon, Portugal

Budapest, Hungary

Zagreb, Croatia

Athens, Greece

Centurion, South Africa

Bucuresti, Romania

Full time

R1571281

Please note that, due to sponsor requirements, we will only consider candidates with experience in MASH, MASLD or Nonalcoholic Steatohepatitis.

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

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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