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
As 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
- 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 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 zł225,500.00 - zł418,600.00. 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.Skills Required
- Bachelor's degree in Life Sciences, Healthcare or 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
IQVIA Compensation & Benefits Highlights
The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about IQVIA and has not been reviewed or approved by IQVIA.
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Healthcare Strength — Healthcare coverage is positioned as comprehensive, spanning medical/dental/vision plus programs like telemedicine, EAP resources, and additional insurance options. Feedback suggests the health offering is a meaningful part of the overall rewards package, though details can vary by location and plan design.
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Retirement Support — Retirement benefits include an employer match structure that supports employee contributions through a defined formula. This adds steady long-term value to total rewards beyond base salary.
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Leave & Time Off Breadth — Time off offerings include vacation/paid time off, holidays, and flexibility themes, with some roles described as having discretionary or unlimited time-off models. This can make the package feel more attractive even when cash compensation is viewed as only mid-range.
IQVIA Insights
What We Do
IQVIA (NYSE:IQV) is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. IQVIA creates intelligent connections across all aspects of healthcare through its analytics, transformative technology, big data resources and extensive domain expertise. IQVIA Connected Intelligence™ delivers powerful insights with speed and agility — enabling customers to accelerate the clinical development and commercialization of innovative medical treatments that improve healthcare outcomes for patients. With approximately 70,000 employees, IQVIA conducts operations in more than 100 countries. To learn more, visit www.iqvia.com.
