Top 19 Clinical trial manager Jobs in Mesa, Az

Senior Global Clinical Study Manager
IQVIA —Gilbert, AZ
- $93,100 - $232,800 a year
- Full-time
- Remote
- Bachelor's degree
- Continuous improvement
- Mentoring
- Work from home
Manager – Imaging Clinical Trial Management Systems
Imaging Endpoints —Scottsdale, AZ
- Computer literacy
- Writing skills
- SQL
6d
Associate Manager / Manager / Senior Manager, Clinical Operations
Imaging Endpoints —Scottsdale, AZ
- Writing skills
- Bachelor's degree
- Organizational skills
Manager - Clinical Trials
HonorHealth —Scottsdale, AZ
- Full-time
- Master's degree
- Bachelor's degree
- Recruiting
Clinical Data Manager
Imaging Endpoints —Scottsdale, AZ
- Analysis skills
- Bachelor's degree
- Continuous improvement
9d
Imaging Project Manager
Imaging Endpoints —Scottsdale, AZ
- Writing skills
- Mid-level
- Bachelor's degree
Clinical Research, Clinical Safety Manager
Castle Biosciences —Phoenix, AZ
- Online Application
- Nursing
- Office
- Bachelor's degree
- Health savings account
- Paid holidays
Quick Apply
Manager Sponsor Regulatory Affairs & Institutional Trial Compliance
HonorHealth —Scottsdale, AZ
- Full-time
- Office
- 3 years
- Master's degree
Site Network Manager (North America)
Alimentiv —Phoenix, AZ
- $97,500 - $163,000 a year
- Full-time
- Remote
- Nursing
- 7 years
- Bachelor's degree
Quick Apply
Research Program Manager - Investigator Initiated Studies
HonorHealth —Scottsdale, AZ
- Full-time
- Office
- 3 years
- Master's degree
5d
Project Lead - RUA92307
IQVIA —Phoenix, AZ
- $200,000 - $225,000 a year
- Full-time
- Nursing
- Driver's License
- Travel
1d
Manager/Senior Manager, Change and Project Management
Imaging Endpoints —Scottsdale, AZ
- Bachelor's degree
- Travel
- Mentoring
Senior Imaging Project Manager
Imaging Endpoints —Scottsdale, AZ
- Writing skills
- Bachelor's degree
- Mentoring
CRC Operations Lead
The Specialty Alliance —Phoenix, AZ
- Full-time
- Writing skills
- Office
- Business development
Quick Apply
Mental Health Clinical Supervisor
Thrivewell Health Centers —Glendale, AZ
- $78,000 - $82,000 a year
- Full-time
- Experience working with individuals with developmental disabilities
- HIPAA
- Experience working with children
- Health insurance
Quick Apply
12d
Project Manager, Clinical Strategy
LifeStance Health —Scottsdale, AZ
- $100,000 - $120,000 a year
- Full-time
- Mid-level
- Bachelor's degree
- Organizational skills
- Paid parental leave
- AD&D insurance
Quick Apply
13d

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Project Lead - RUA92307
IQVIA —Phoenix, AZ
Master’s degree required in social work, mental health counseling, psychology, nursing, public health, health sciences, or a related healthcare field; advanced…
$200,000 - $225,000 a year
1d
Lead Clinical Research Coordinator
ECN Operating LLC —Sun City, AZ
Bachelor’s degree in health sciences, life sciences, nursing, or related field required. Ensure timely and accurate data entry into electronic data capture (EDC…
Quick Apply
11d

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Senior Global Clinical Study Manager

IQVIA -
Gilbert, AZ

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

Gilbert, 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

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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