ZipRecruiter

Log In

1

Senior Clinical Study Manager Jobs (NOW HIRING)

ShiftCode Analytics

Clinical Study Lead

Tarrytown, NY · On-site

Clinical Study Lead The Temp Senior Clinical Study Lead (CSL) Clinical Experimental Sciences ... This role may be responsible for direct line management. This role has a 3-day minimum onsite ...

New

IQVIA

Senior Global Clinical Study Manager

Tampa, FL · On-site

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 ...

IQVIA

Senior Global Clinical Study Manager

Chicago, IL · On-site

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 ...

IQVIA

Senior Global Clinical Study Manager

New York, NY · On-site

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 ...

IQVIA

Senior Global Clinical Study Manager

Tampa, FL · On-site

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 ...

IQVIA

Senior Global Clinical Study Manager

Gilbert, AZ · On-site

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 ...

next page

Showing results 1-20

All JobsSenior Clinical Study Manager Jobs

Senior Clinical Study Manager information

See salary details

$22K

$125.3K

$206K

How much do senior clinical study manager jobs pay per year?

As of Jul 6, 2026, the average yearly pay for senior clinical study manager in the United States is $125,290.00, according to ZipRecruiter salary data. Most workers in this role earn between $85,000.00 and $157,000.00 per year, depending on experience, location, and employer.

What does a Senior Clinical Study Manager do?

A Senior Clinical Study Manager oversees the planning, execution, and management of clinical trials to ensure they comply with regulatory standards and meet study objectives. They coordinate with cross-functional teams, manage study timelines and budgets, and ensure data integrity. Additionally, they are responsible for monitoring the progress of trials, resolving issues that arise, and communicating results to stakeholders. Their role is critical for advancing medical research and ensuring that new treatments are safe and effective.

How does a Senior Clinical Study Manager typically collaborate with cross-functional teams during a study?

A Senior Clinical Study Manager works closely with cross-functional teams such as data management, regulatory affairs, biostatistics, medical writing, and clinical operations to ensure smooth study execution. They facilitate regular meetings, coordinate timelines, and address challenges that arise across teams, ensuring everyone aligns with study objectives and regulatory standards. This role often requires strong communication and leadership skills to manage dependencies, resolve conflicts, and keep projects on track. Effective collaboration is key to maintaining study quality and meeting project milestones.

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

To thrive as a Senior Clinical Study Manager, you need in-depth knowledge of clinical trial processes, regulatory guidelines (such as GCP and ICH), and a relevant life sciences degree, often complemented by several years of clinical research experience. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and certifications like ACRP or SOCRA are typically required. Strong leadership, organizational, and communication skills help manage cross-functional teams and ensure effective collaboration with stakeholders. These skills are essential for delivering high-quality, compliant studies on time and within budget, ultimately supporting successful drug development.
More about Senior Clinical Study Manager jobs
What cities are hiring for Senior Clinical Study Manager jobs? Cities with the most Senior Clinical Study Manager job openings:
Who are the top companies hiring for Senior Clinical Study Manager jobs? The top employers for Senior Clinical Study Manager jobs are:
What states have the most Senior Clinical Study Manager jobs? States with the most job openings for Senior Clinical Study Manager jobs include:
What job categories do people searching Senior Clinical Study Manager jobs look for? The top searched job categories for Senior Clinical Study Manager jobs are:
What are popular job titles related to Senior Clinical Study Manager jobs? For Senior Clinical Study Manager jobs, the most frequently searched job titles are:
Senior Clinical Study Manager jobs near you
Infographic showing various Senior Clinical Study Manager job openings in the United States as of June 2026, with employment types broken down into 76% Full Time, 18% Part Time, and 6% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $125,290 per year, or $60.2 per hour.
Senior Global Clinical Study Manager

Senior Global Clinical Study Manager

IQVIA

New York, NY

Full-time

Posted 12 days ago

IQVIA rating

8.1

Company rating: 8.1 out of 10

Based on 53 frontline employees who took The Breakroom Quiz

53rd of 207 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

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom

IQVIA logo

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

View All IQVIA Jobs

Apply