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Global Study Manager Jobs in Indiana (NOW HIRING)

Elanco

Senior Product Manager - Global Web

Indianapolis, IN · Hybrid

$120K - $159K/yr

Senior Product Manager, Global Web Products As the Senior Product Manager for Global Web Products ... Studies have shown underrecognized groups are less likely to apply to jobs unless they meet every ...

Eurofins

Global Sample Management Specialist

Indianapolis, IN · On-site

$91K - $111K/yr

... clinical studies, as well as having an emerging global presence in Contract Development and ... Strong time/task management skills Additional Information * Position is full-time, working Monday ...

Becton, Dickinson and Company

$139K/yr

Waters Biosciences is looking for a strategic, data-driven Global Product Marketing Manager to lead ... Develop customer-facing content-brochures, case studies, economic value calculators and web content ...

Allegion

VP, Global Procurement

Carmel, IN · On-site

Materials management experiences either through direct management, projects, or programs. * Applies ... Studies have shown that some people are less likely to apply to jobs unless they meet every single ...

Allegion

VP, Global Procurement

Carmel, IN · On-site

Materials management experiences either through direct management, projects, or programs. * Applies ... Studies have shown that some people are less likely to apply to jobs unless they meet every single ...

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Global Study Manager information

See Indiana salary details

$21.9K

$58.4K

$97.5K

How much do global study manager jobs pay per year?

As of Jul 16, 2026, the average yearly pay for global study manager in Indiana is $58,379.00, according to ZipRecruiter salary data. Most workers in this role earn between $41,900.00 and $65,700.00 per year, depending on experience, location, and employer.

How much does a global study manager make?

A global study manager typically earns between $80,000 and $150,000 annually, depending on experience, location, and the size of the organization. They often require strong project management skills and knowledge of clinical research or related fields.

What jobs pay 200,000 a year in the USA?

In the USA, roles like Global Study Manager, senior medical directors, software engineers, and executive-level positions in finance or law often have salaries of $200,000 or more annually. These positions typically require advanced degrees, extensive experience, and specialized skills, and may involve leadership responsibilities or technical expertise.

What are the key skills and qualifications needed to thrive as a Global Study Manager, and why are they important?

To excel as a Global Study Manager, you need expertise in clinical trial management, regulatory requirements, and project leadership, often backed by a life sciences degree and experience in global studies. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and GCP certification are commonly required. Excellent organizational skills, cross-cultural communication, and problem-solving abilities are vital soft skills for this role. These skills ensure effective coordination of international studies, compliance with regulations, and the successful delivery of complex clinical projects.

What jobs pay 500,000 a year in the US?

In the US, high-paying roles such as senior executives, investment bankers, specialized surgeons, and certain technology executives can earn $500,000 or more annually. These positions often require advanced degrees, extensive experience, and leadership responsibilities, with compensation including base salary, bonuses, and stock options.

How does a Global Study Manager collaborate with cross-functional teams during a clinical trial?

A Global Study Manager plays a pivotal role in coordinating with cross-functional teams, such as clinical operations, data management, regulatory affairs, and safety teams, to ensure smooth execution of clinical trials. They facilitate regular meetings, provide clear communication on study timelines and deliverables, and address any issues that arise across different geographic regions. Effective collaboration is crucial for aligning global processes, maintaining data consistency, and meeting regulatory requirements, making strong interpersonal and project management skills essential for success in this role.

What does a global study manager do?

A global study manager oversees the planning, execution, and management of clinical research studies across multiple regions or countries. They coordinate with cross-functional teams, ensure compliance with regulatory requirements, and monitor study progress using project management tools to meet deadlines and quality standards.
What are popular job titles related to Global Study Manager jobs in Indiana? For Global Study Manager jobs in Indiana, the most frequently searched job titles are:
What job categories do people searching Global Study Manager jobs in Indiana look for? The top searched job categories for Global Study Manager jobs in Indiana are:
What cities in Indiana are hiring for Global Study Manager jobs? Cities in Indiana with the most Global Study Manager job openings:
Global Study Manager jobs near you
Senior Global Clinical Study Manager

Senior Global Clinical Study Manager

IQVIA

Indianapolis, IN • On-site

Full-time

Posted 21 days ago

IQVIA rating

8.1

Company rating: 8.1 out of 10

Based on 53 frontline employees who took The Breakroom Quiz

56th of 210 rated it services

Job description

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 ResponsibilitiesGlobal 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
QualificationsRequired
  • 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 athttps://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.

What IQVIA employees say

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Benefits

Hours and flexibility

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About IQVIA

Sourced by ZipRecruiter

At IQVIA, we are passionate about helping customers and partners improve results and patient outcomes. Everything we do contributes to this vision for creating a healthier world. In today’s healthcare environment, it’s not only about how much data, information, and technology you have at your fingertips – it’s what you do with it. IQVIA is focused on making intelligent connections for customers across the entire healthcare ecosystem to help you drive healthcare forward. Whether that means partnering with novel technology companies to boost patient engagement, leveraging AI & machine learning to accelerate results, or using decentralized trials to reach the right patients wherever they are – we are always looking for smarter ways to move you forward.

Industry

Health care and social assistance

Company size

10,000+ Employees

Headquarters location

Durham, NC, US

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