Senior Clinical Project Manager (CAR-T)

IQVIA LLC; Durham, Northern (NC, KY); On-site; USD 93,000 - 233,000; Full time

Job summary

IQVIA LLC is seeking a Senior Clinical Project Manager to lead global studies, partnering with sponsors and cross-functional teams to drive study delivery and operational excellence.

You will oversee multi-regional trials, ensure compliance with ICH-GCP and regulatory requirements, manage timelines and budgets, and mentor regional leaders. This role offers high-impact leadership within a global CRO/biotech context.

Qualifications

• Bachelor's degree in Life Sciences, Healthcare or related scientific discipline.
• 7+ years of clinical research experience with global or multi-regional trials.
• Solid knowledge of ICH-GCP guidelines and regulatory requirements.

Responsibilities

• Lead delivery of complex global and multi-regional studies, driving timelines, budgets, quality and risk management.
• Serve as primary strategic partner for sponsors, providing leadership and solutions for study success.
• Provide leadership to cross-functional teams across regions, driving collaboration and high performance.
• Oversee study timelines, budgets, quality, risks and operational delivery to ensure study success.
• Drive proactive risk management, issue resolution and stakeholder alignment throughout the study lifecycle.
• Ensure studies comply with ICH-GCP and contractual commitments.

Skills

Cross-functional leadership

Sponsor relationship management

Risk management

Budget & timeline management

ICH-GCP knowledge

Global project leadership

Education

Bachelor's degree in Life Sciences/Healthcare/related

Job description

Senior Clinical Project Manager - Global Study Leadership

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 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, 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 Doing

• 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
• 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 IQVIA

If you're looking for a role that combines global exposure, strategic leadership, sponsor partnership and meaningful work, we'd love to hear from you. At IQVIA, you'll have the opportunity to work on high-profile global studies, collaborate with industry-leading sponsors, leverage cutting-edge technology and build a rewarding career with one of the world's leading clinical research organizations, all while helping bring innovative treatments to patients faster.

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 proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law.

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.

The potential base pay range for this role, when annualized, is $93,100.00 - $232,800.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time).

• Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

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.