Senior Global Clinical Study Manager
Job Location:
Durham, NC - USA
Monthly Salary:
Posted on:
Vacancies:
Job Summary
IQVIA Biotech is a full-service CRO purpose-built to serve biotech sponsors. With over 25 years of experience we offer agile therapeutically aligned solutions and trusted partnerships that help bring breakthrough treatments to patients faster.
Drive global clinical trials from first site activation to final patient visitown the strategy accelerate delivery and shape the future of clinical research worldwide.
Required Experience
- 2 years of global study management experience
- Experience across multiple countries/regions
- Phase IIII clinical trials experience (Phase III required)
- Oncology experience required
- Ability to work across multiple therapeutic areas
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 closeoutwhile 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
Global Study & Site Leadership
- 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
Project & Stakeholder Management
- 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
Operational Excellence & Risk Management
- 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
Financial & Contract Management
- 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)
Quality & Compliance
- Maintain TMF health and ensure timely document submission
- Develop quality monitoring plans and compliance metrics
- Ensure adherence to study tools training materials and processes
Team Leadership & Development
- 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
Required
- Bachelors 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
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
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. 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 $93100.00 - $232800.00. 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.Required Experience:
Manager
About Company
IQVIA is the Human Data Science Company™. We are inspired by the industry we serve and provide solutions that enable life sciences companies to innovate with confidence, maximize opportunities and ultimately drive human health outcomes forward. Our approach is Human Data Science – a d ... View more
