Senior Global Clinical Study Manager

IQVIA

Tampa, FL

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JOB DETAILS

SALARY

$93,100–$232,800 Per Year

SKILLS

Billing, Biology, Budget Management, Change Requests/Orders, Clinical Information Systems, Clinical Monitoring, Clinical Practices/Protocols, Clinical Research, Clinical Trial, Clinical Trial Management, Continuous Improvement, Contract Management, Corrective Action, Cross-Functional, Customer Relations, Customer Support/Service, Data Quality, Detail Oriented, Electronic Data Capture (EDC), Expense Tracking, FDA Requirements, Financial Management, Financial Projections, Forecasting, GCP (Good Clinical Practices), Health Maintenance, Healthcare, ICH Regulations, Leadership, Maintain Compliance, Management Strategy, Matrix Management, Medical Treatment, Mentoring, Metrics, Microsoft Office, Oncology, Operational Strategy, Patient Care, Performance Analysis, Phase I Clinical Trials, Phase III Clinical Trials, Problem Solving Skills, Quality Metrics, Quality Monitoring, Regulations, Regulatory Requirements, Research Protocols, Revenue Forecasting, Risk Analysis, Risk Management, Standard Operating Procedures (SOP), Team Lead/Manager, Time Management, Trend Analysis

LOCATION

Tampa, FL

POSTED

4 days ago

_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 visit—own 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 I–III 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 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** **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** + 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 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. 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. 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. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. 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. EEO Minorities/Females/Protected Veterans/Disabled

About the Company

IQVIA

IQVIA™ is The Human Data Science Company™, focused on using data and science to help healthcare clients find better solutions for their patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness advances in healthcare information, technology, analytics and human ingenuity to drive healthcare forward. Healthcare is an industry designed to help humans. As a global community, we continuously invest and commit to advancing human health. To deliver value and real outcomes. To rise to the challenge to find the next breakthrough by making the most of increasingly limited resources. We are inspired by the potential and propelled by the possibilities. We share the vision to drive healthcare forward. To see how we can help accelerate progress and achievements. Others are developing these medical breakthroughs. We do our part by using breakthroughs in insights, technology and human intelligence to reimagine and deliver ways to help make them a reality. It’s bigger than better clinical trials. Or advances in technologies and analytics. Or faster insights. It’s about exploring a new path to better health outcomes via Human Data Science. It’s about harnessing the power of the IQVIA CORE™ to channel the insights, commercial and scientific depth, and executional expertise that drive maximum value for our customers. Motivated by the industry we help, we’re committed to providing solutions that enable life sciences companies to innovate with confidence, maximize opportunities, and, ultimately, drive human health outcomes forward.

COMPANY SIZE

10,000 employees or more

INDUSTRY

Healthcare Services

FOUNDED

1982

WEBSITE

https://www.iqvia.com/

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