Clinical Project Management Director, Cell & Gene Therapy - Global Study Leadership
IQVIA · BE
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About the Role
Lead complex global oncology programs and partner with senior stakeholders to shape the future of cancer research. This strategic leadership role offers the opportunity to influence development strategy, drive operational excellence, and oversee the successful execution of innovative clinical studies.
Responsibilities
- Lead the delivery of large, complex global clinical studies and multi-study programs, translating customer objectives into effective operational strategies and execution plans.
- Provide operational leadership across programs and portfolios, ensuring consistency, quality, financial performance, and successful delivery of clinical milestones.
- Serve as the primary senior contact for sponsors, building trusted relationships, managing escalations, and driving collaborative solutions.
- Lead and align global, matrixed teams across clinical operations, data management, safety, regulatory, and other functional areas.
- Proactively identify operational and strategic risks, implement mitigation plans, and lead issue resolution efforts.
- Oversee program financial performance, resource planning, forecasting, scope management, and change control activities.
- Contribute to proposal development, strategic planning, and bid defense activities for large, multi-service clinical opportunities.
- Drive innovation, process optimization, and the implementation of best practices.
- Mentor and develop project leaders and cross-functional team members, fostering a culture of accountability, collaboration, and professional growth.
Requirements
- 12-15+ years of experience in clinical research, clinical operations, and/or project leadership within the pharmaceutical, biotechnology, or CRO industry.
- Substantial experience leading large, global Phase I-IV oncology studies and development programs.
- Deep oncology therapeutic expertise is required.
- Strong preference for experience leading Cell & Gene Therapy (CGT), CAR-T, TCR-T, gene editing or other Advanced Therapy Medicinal Product (ATMP) programs.
- Demonstrated success leading complex global oncology portfolios and building trusted relationships with executive-level stakeholders.
- Proven success leading large, global, multi-regional clinical studies, programs or portfolios with operational and financial responsibility.
- Strong understanding of clinical trial conduct, ICH-GCP guidelines and applicable regulatory requirements.
- Demonstrated ability to build and maintain executive-level customer relationships and successfully manage complex stakeholder environments.
- Experience leading matrixed, cross-functional teams in a global environment.
- Strong strategic thinking, problem-solving and risk management capabilities.
- Excellent communication, presentation and influencing skills.
- Bachelor's degree in Life Sciences or a related field required; advanced degree preferred.
Skills
- Oncology expertise
- Cell & Gene Therapy (CGT)
- CAR-T
- TCR-T
- Gene editing
- Advanced Therapy Medicinal Product (ATMP)
- Clinical trial conduct
- ICH-GCP guidelines
- Regulatory requirements
- Strategic thinking
- Problem-solving
- Risk management
- Communication
- Presentation
- Influencing
Experience Level
- 12-15+ years of experience
Education Level
- Bachelor's degree in Life Sciences or a related field
- Advanced degree preferred
Salary/Compensations
- $125,900.00 - $350,900.00
About the Company
- 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
Equal Opportunity
- 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.
- https://jobs.iqvia.com/eoe
- 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.