Top 15 Clinical study manager Jobs in Indianapolis, In

Senior Global Clinical Study Manager
IQVIA —Indianapolis, IN
- $93,100 - $232,800 a year
- Full-time
- Remote
- Bachelor's degree
- Continuous improvement
- Mentoring
- Work from home
Clinical Data Manager (P3)
Eli Lilly —Indianapolis, IN
- $154,306.00 - $177,451.90 a year
- Full-time
- Azure
- Computer Science
- Mid-level
- Health insurance
- Dental insurance
Clinical Research Coordinator
Community Health Network —Indianapolis, IN
- Full-time
- Mid-level
- Clinic
- Associate's degree
7d
Senior Clinical Research Associate (level dependent on experience)
CTI Clinical Trial Services, Inc —Indianapolis, IN
- Hybrid work
- Nursing
- Mid-level
- Master's degree
- Paid parental leave
- Tuition reimbursement
Quick Apply
Clinical Research Management System Study Specialist (IT Project Management Specialist)
Indiana University —Indianapolis, IN
- Full-time
- Mid-level
- Bachelor's degree
- Computer skills
- Paid parental leave
- Health savings account
6d
Study Design Lead – Clinical Research , Central Labs Services
Labcorp —Indianapolis, IN
- $70,000 - $90,000 a year
- Full-time
- High school diploma or GED
- Bachelor's degree
- Fair chance
- Employee stock purchase plan
- Disability insurance
12h
Clinical Data Manager (P3)
Information Technology Senior Management Forum —Indianapolis, IN
- $154,306.00 - $177,451.90 a year
- Part-time
- Azure
- Computer Science
- Mid-level
- Health insurance
- Dental insurance
Regional Study Coordinator - Central Labs Services - Clinical Research
Labcorp —Indianapolis, IN
- $60,000 - $65,000 a year
- Full-time
- Mid-level
- High school diploma or GED
- Bachelor's degree
- Employee stock purchase plan
- Disability insurance
1d
Clinical Research Coordinator
Indiana University —Indianapolis, IN
- $55,848.00 - $74,006.40 a year
- Full-time
- 5 years
- Mid-level
- Databases
- Paid parental leave
- Health savings account
18h
Clinical Research Monitor (Quality Control Specialist)
Indiana University —Indianapolis, IN
- Full-time
- Hybrid work
- Office
- 3 years
- Analysis skills
- Paid parental leave
- Health savings account
2d
Research Quality Assurance Manager
Innovative Hematology, Inc. —Indianapolis, IN
- Hybrid work
- 5 years
- Master's degree
- Analysis skills
Quick Apply
13d
Project Lead Data Manager
Elanco —Indianapolis, IN
- Full-time
- Hybrid work
- 5 years
- Bachelor of Science
- Office
- Paid time off
- Parental leave
Study Participant Recruiter
Headlands Research —Indianapolis, IN
- $21 - $24 an hour
- Temporary
- Spanish
- HIPAA
- English
- Health savings account
- Disability insurance
Quick Apply
Senior Data Manager
Labcorp —Indianapolis, IN
- $75,000 - $95,000 a year
- Full-time
- Mentoring
- Fair chance
- Senior level
- Employee stock purchase plan
- Disability insurance
6d

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Clinical Data Manager (P3)
Eli Lilly —Indianapolis, IN
Position requires a Bachelor’s degree in Data Science, Electronic Engineering, Computer Science, or a related STEM field and 3 years of experience with clinical…
$154,306.00 - $177,451.90 a year
Clinical Data Manager (P3)
Information Technology Senior Management Forum —Indianapolis, IN
Position requires a Bachelor’s degree in Data Science, Electronic Engineering, Computer Science, or a related STEM field and 3 years of experience with clinical…
$154,306.00 - $177,451.90 a year

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Senior Global Clinical Study Manager

IQVIA -
Indianapolis, IN

Apply Now

Job Details

Full-time
$93,100 - $232,800 a year

Benefits

Work from home

Qualifications

Clinical program budget management
Customer communication
Regulatory compliance
Global team management
ICH guidelines
Bachelor's degree
Project management experience in healthcare
Managing clinical research teams
Oncology research
Healthcare financial management
Clinical quality assurance standards
Oncology
Healthcare compliance
Operational budget management
Leading research teams
FDA regulations

Full Job Description

Indianapolis, United States of America | Full time | Home-based | R1553750

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.

Where you'll work

Home-based

You’ll work remotely, with the flexibility to do your best work from home. Supported by collaborative tools and a global team, you’ll stay connected while enjoying the autonomy and balance that comes with a fully remote role.

Culture

Culture at IQVIA is built on a shared belief: that when people are empowered with better data, smarter technology and deeper expertise, they can change what’s possible for patients. Across every team and every corner of the globe, you’ll find colleagues who genuinely care — about the mission and about each other. That’s what makes this a place where people tend to stay, grow and do the best work of their careers.

Apply Now

Refine Your Search

clinical study manager jobs in indianapolis, in

Senior Global Clinical Study Manager

Clinical Data Manager (P3)

Clinical Research Coordinator

Senior Clinical Research Associate (level dependent on experience)

Clinical Research Management System Study Specialist (IT Project Management Specialist)

Study Design Lead – Clinical Research , Central Labs Services

Clinical Data Manager (P3)

Regional Study Coordinator - Central Labs Services - Clinical Research

Clinical Research Coordinator

Clinical Research Monitor (Quality Control Specialist)

Research Quality Assurance Manager

Project Lead Data Manager

Study Participant Recruiter

Senior Data Manager

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Required Experience

Job Overview

Key Responsibilities

Global Study & Site Leadership

Project & Stakeholder Management

Operational Excellence & Risk Management

Financial & Contract Management

Quality & Compliance

Team Leadership & Development

Qualifications

Required

Core Competencies

Why Join Us

Where you'll work

Home-based

Culture

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