Senior Global Clinical Study Manager
Job Overview
We are seeking a Global Study Manager responsible for the end-to-end planning, execution, and delivery of clinical trial site management activities across global studies. This role ensures successful site selection, activation, monitoring oversight, and closeout—while balancing speed, quality, and cost. You will serve as the primary point of contact for clients, lead cross-functional teams, and ensure compliance with ICH-GCP, regulatory requirements, and study protocols. This is a highly visible role that combines strategic leadership, operational execution, and financial oversight.
Key Responsibilities
Lead site management strategy from study award through close-out
Oversee site identification, selection, activation, and recruitment performance
Ensure clinical monitoring processes meet study needs and timelines
Partner with CRAs to optimize enrollment, data quality, and compliance
Serve as primary client contact and own key customer relationships
Lead cross-functional teams across regions and cultures
Facilitate internal and external meetings, including executive presentations
Drive collaboration across stakeholders, vendors, and functional leads
Develop and manage integrated study plans and risk mitigation strategies
Proactively identify risks and implement corrective/preventative actions
Monitor study timelines, enrollment trends, and data quality metrics
Ensure compliance with GCP, SOPs, protocols, and regulatory standards
Manage study financials, including forecasting and revenue acceleration
Identify and manage out-of-scope work and change orders
Oversee Billing Unit Reviews (BURs) and expense approvals
Track performance against budget and Estimate at Completion (EAC)
Maintain TMF health and ensure timely document submission
Develop quality monitoring plans and compliance metrics
Ensure adherence to study tools, training materials, and processes
Lead and mentor cross-functional project teams
Support CRA and team training on therapeutic areas and study-specific needs
Foster collaboration, knowledge sharing, and continuous improvement
Qualifications
Bachelor’s degree in life sciences or related field
5+ years of clinical research/monitoring experience, including 2 years in a clinical study management role
Strong knowledge of ICH-GCP, FDA regulations, and clinical trial processes
Experience managing global clinical trials and multi-regional teams
Demonstrated experience in project financial management
Core Competencies
Exceptional communication and stakeholder management skills
Strong problem-solving and risk mitigation capabilities
Ability to influence without authority in matrix organizations
High attention to detail and quality-driven mindset
Proficiency in Microsoft Office and clinical systems (e.g., CTMS, EDC)
Why Join Us
Work on cutting-edge global trials across therapeutic areas
Collaborate with top talent in a dynamic, global environment
Make a direct impact on patient outcomes worldwide
About the Role
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.
Company Information
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. Learn more about our commitment to diversity and inclusion.
Equal Opportunity Employer
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.
Pay Range
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).