Senior Clinical Project Manager (Renal, Obesity, MASH) - Global Study Leadership

Job Title: Senior Clinical Project Manager (Renal, Obesity, MASH) - Global Study Leadership

Job Location: London, Greater London, United Kingdom

Job Location Type: Remote

Job Contract Type: Full-time

Job Seniority Level: At IQVIA, our Senior Project Managers play a pivotal role in bringing innovative medicines to patients worldwide. You'll provide strategic leadership for complex global clinical trials, partnering directly with sponsors and cross-functional teams to deliver studies that accelerate the development of life-changing therapies.

This is an opportunity to lead large-scale, multi-regional studies focused on renal, obesity and/or MASH (Metabolic Dysfunction-Associated Steatohepatitis) for some of the world's most innovative pharmaceutical and biotechnology companies while expanding your leadership impact and helping shape the future of clinical research.

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 on some of the industry's most complex global clinical trials, partnering directly with leading pharmaceutical and biotechnology sponsors across therapeutic areas including Oncology, Rare Disease, CNS, Cardiovascular, Immunology, Respiratory, Renal, Obesity, MASH (Metabolic Dysfunction-Associated Steatohepatitis), Cell & Gene Therapy, Infectious Disease, Ophthalmology and Women's Health. Supported by a collaborative global network, flexible ways of working and AI-enabled technology and data-driven insights, you'll have exceptional opportunities to broaden your expertise, expand your leadership impact and accelerate your career within one of the world's leading clinical research organizations.

What You'll Be DoingAs the strategic leader of your studies, you'll be accountable for the successful delivery of complex global clinical trials from start-up through close-out, ensuring quality, timeline, budget, regulatory and customer objectives are achieved.

Key Responsibilities

• Lead the delivery of complex global and multi-regional clinical studies, driving operational excellence and successful study outcomes

• Serve as the primary strategic partner for sponsors, providing leadership, guidance and innovative solutions to drive successful study outcomes

• Provide leadership and direction to cross-functional teams across regions, fostering collaboration, accountability and high performance

• Oversee study timelines, budgets, quality, risks, financial performance and operational delivery to ensure study success

• Drive proactive risk management, issue resolution, decision-making and stakeholder alignment throughout the study lifecycle

• Ensure studies are delivered in compliance with ICH-GCP, regulatory requirements and contractual commitments

What We're Looking For

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

• 7+ years of clinical research experience, including significant project management experience leading global or multi-regional clinical trials within a CRO, pharmaceutical or biotechnology environment

• Experience leading renal, obesity and/or MASH (Metabolic Dysfunction-Associated Steatohepatitis) global clinical studies is strongly preferred

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

• Proven success leading cross-functional teams and managing study delivery, including timelines, budgets, quality, risks and operational performance

• Demonstrated ability to build trusted sponsor relationships and effectively manage senior stakeholders in a global environment

• Exceptional leadership, communication, problem-solving and decision-making skills

• Passion for advancing clinical research and improving patient outcomes

Build Your Future with IQVIAIf you're looking for a role that combines global exposure, strategic leadership, sponsor par...