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Global Study Manager Jobs (NOW HIRING)

Suvoda

Travel & Customer Service Coordinator

$18.50 - $24/hr

The Global Studies Coordinator (based in the United States) is responsible for supporting the team of Global Study Managers in the planning and operations of active clinical trial studies. The ...

ICON

Country Study Operations Manager

Blue Bell, PA · On-site +1

Country Study Operations Manager- Remote ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a ...

Icon plc

Country Study Operations Manager

Blue Bell, PA · On-site

Country Study Operations Manager- Remote ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a ...

ARTHREX

Sr. Clinical Study Manager

Naples, FL

This is an onsite position based at our global headquarters in Naples, Florida. Essential Duties and Responsibilities: * Leading, planning, executing, managing, and oversight of clinical studies ...

Intuitive

Senior Clinical Study Manager

Sunnyvale, CA · On-site +1

As a global leader in robotic-assisted surgery and minimally invasive care , our technologies-like ... This Lead Clinical Study Manager-4 (CSM IV) / Senior Clinical Study Manager role will develop and ...

Intuitive

Senior Clinical Study Manager

Sunnyvale, CA · On-site

As a global leader in robotic-assisted surgery and minimally invasive care , our technologies-like ... This Lead Clinical Study Manager-4 (CSM IV) / Senior Clinical Study Manager role will develop and ...

Arthrex

Sr. Clinical Study Manager

Naples, FL · On-site

Join our talented team at a global medical device company focused on Helping Surgeons Treat Their ... Manages site initiation activities (e.g., study start-up documentation preparation) * Responsible ...

Danaher

Senior Clinical Study Manager

As a global leader with the most comprehensive portfolio spanning from biopsy to diagnosis, we ... The Senior Clinical Study Manager is responsible for clinical trial execution within the US and EU ...

TEEMA

Study Manager - Mining & Metals

Phoenix, AZ · On-site

$90K - $145K/yr

We are seeking a high-caliber Study Manager to lead complex Pre-Feasibility (PFS) and Feasibility Studies (FS) for a global ECPM leader. Based in our Phoenix center of excellence , you will guide ...

Glaukos

Manager Study Start-up

San Clemente, CA

Our global headquarters is in Aliso Viejo, California with additional locations in San Clemente ... Clinical Study Manager The Clinical Study Manager is responsible for the end-to-end management and ...

Arthrex

Clinical Study Manager

Naples, FL · On-site

Clinical Study Manager Arthrex, Inc. is a global medical device company and a leader in new product development and medical education in orthopedics. Arthrex is actively searching for a Clinical ...

ARTHREX

Clinical Study Manager

Naples, FL

Clinical Study Manager Arthrex, Inc. is a global medical device company and a leader in new product development and medical education in orthopedics. Arthrex is actively searching for a Clinical ...

Glaukos

Manager Study Start-up

San Clemente, CA · On-site

Our global headquarters is in Aliso Viejo, California with additional locations in San Clemente ... Clinical Study Manager The Clinical Study Manager is responsible for the end-to-end management and ...

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Global Study Manager information

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$23K

$61.4K

$102.5K

How much do global study manager jobs pay per year?

As of Aug 7, 2026, the average yearly pay for global study manager in the United States is $61,351.00, according to ZipRecruiter salary data. Most workers in this role earn between $44,000.00 and $69,000.00 per year, depending on experience, location, and employer.

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.

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.
More about Global Study Manager jobs
What cities are hiring for Global Study Manager jobs? Cities with the most Global Study Manager job openings:
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Global Study Manager jobs near you
Infographic showing various Global Study Manager job openings in the United States as of August 2026, with employment types broken down into 88% Full Time, 11% Part Time, and 1% Contract. Highlights an 85% Physical, 2% Hybrid, and 13% Remote job distribution, with an average salary of $61,351 per year, or $29.5 per hour.

Travel & Customer Service Coordinator

Suvoda

Remote

$18.50 - $24/hr

Part-time, Contractor

Posted 15 days ago

Job description

We know why you are reading about this opportunity. You are driven to achieve goals. You are looking to make a direct impact. You want to work in a culture where your co-workers work as part of a diverse team, communicate across departments, and have a positive attitude. If we had to guess, you are innovative with great ideas, want to bring efficiencies to processes, and are looking to grow your career. Are we right? If so, let's talk more!
The Global Studies Coordinator (based in the United States) is responsible for supporting the team of Global Study Managers in the planning and operations of active clinical trial studies. The Coordinator is the main point of contact for patient communications and the management of all patient travel and logistical details.
Please note: The internal title for this role is 'Global Study Coordinator.' This is a contract position. It is part-time, potentially up to 25 hours per week, and pays on an hourly basis. Hours are not guaranteed.
Responsibilities:
  • Manages travel and transportation budget for trial participants
  • Participates in discussions with vendors and internal team members regarding trial participant requirements
  • Supports hospital or clinical staff relating to trial participant enrollments and visit schedules
  • Promptly responds to all inquiries of the trial participants and hospital/clinical staff
  • Contributes to managing projects to profitable level through efficient work process
  • Acts as point of contact for patient communication regarding air, hotel and ground accommodations
  • Maintains accurate data including setting up databases and transferring data between internal operating systems
  • Aids in producing reports as required
  • Works with Global Study Manager to outline needs and requests of clients and patients
  • Contributes to managing projects to profitable level through efficient work process

Requirements:
  • Bachelor's Degree or equivalent work experience
  • Fluent Spanish and fluent English required, multi-lingual preferred
  • 2+ years of experience in the travel industry and/or pharma industry preferred
  • Working knowledge of Microsoft Office
  • Ability to learn new procedures quickly and efficiently
  • Highly organized and plan-oriented; adept at prioritization and follow-up
  • Excels in cross-departmental communication
  • Confidence and follow through in decision-making

Working Conditions:
  • Primary work environment is from a home office with personal computer and telephone
  • Minimum technology required, including updated operating system, anti-virus software and password protected devices. Chromebook is not supported.

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As set forth in Suvoda's Equal Employment Opportunity policy, we do not discriminate on the basis of any protected group status under any applicable law.
If you are based in California, we encourage you to read this important information for California residents linked here.

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