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Global Trial Manager Jobs (NOW HIRING)

Clinical Trial Manager

Philadelphia, PA · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Clinical Trial Manager - Phase I oncology ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As ...

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Clinical Trial Manager - Phase I oncology ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As ...

Global Trial Optimization Specialist

Blue Bell, PA · On-site +1

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Global Trial Optimization Specialist - Gen Med/Infectious Disease Vaccines - Home Based (US) ICON ... Manage the scope of work, objectives, quality of deliverables, and other activities of assigned ...

Global Trial Optimization Specialist

Blue Bell, PA · On-site +1

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Global Trial Optimization Specialist - Gen Med/Infectious Disease Vaccines - Home Based (US) ICON ... Manage the scope of work, objectives, quality of deliverables, and other activities of assigned ...

BA/BS with 7+ years of experience in global clinical trial management roles from pharmaceutical companies and/or CROs * Experience within the field of cardiovascular studies and/or rare disease is ...

Experience managing global Phase 1-3 trials and vendor/CRO oversight required. * Experience in ... Proficiency with clinical trial systems (e.g., CTMS, eTMF, EDC); experience with SAS a plus.

Clinical Trial Manager

Boston, MA · On-site

$100K - $125K/yr

We are seeking a Clinical Trial Manager with experience in managing a global Phase 3 clinical trial. Works with senior Clinical Operations members to lead the clinical project team members in the ...

Clinical Trial Manager

San Mateo, CA · On-site

$90 - $100/hr

... global Phase 2 and/or Phase 3 clinical trial: start up, treatment phase and database lock. • ... management and oversight of CROs/vendors required. • Experience with double blind/placebo ...

Clinical Trial Manager

Watertown, MA · On-site

$115K - $200K/yr

Contribute to the planning, implementation and execution of a global clinical trial * Responsible for management of vendors to support clinical trial execution * Plan, execute, and lead study ...

... Global Talent Management, Value Added Services through CLASS (Competency Leveraged Advanced ... Qualifications Responsible for supporting the Senior Clinical Trial Manager/operational study lead ...

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Global Trial Manager information

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$28

$62

$96

How much do global trial manager jobs pay per hour?

As of Aug 17, 2026, the average hourly pay for global trial manager in the United States is $62.52, according to ZipRecruiter salary data. Most workers in this role earn between $50.72 and $70.43 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a global trial manager?

To thrive as a Global Trial Manager, you need expertise in clinical trial management, regulatory compliance, and project coordination, typically supported by a degree in life sciences or a related field and experience in clinical research. Familiarity with electronic data capture (EDC) systems, ICH-GCP guidelines, and project management tools is essential, and certifications like PMP or CCRP are often advantageous. Outstanding leadership, cross-cultural communication, and problem-solving skills help manage international teams and stakeholders effectively. These skills are crucial for ensuring complex, multi-country trials run smoothly, on schedule, and in compliance with global standards.

What is a global trial manager?

A Global Trial Manager is a professional responsible for overseeing the planning, execution, and management of clinical trials conducted across multiple countries. They coordinate with cross-functional teams, ensure compliance with regulatory requirements, manage budgets and timelines, and address challenges that arise during the trial process. Their role is critical in ensuring that clinical studies are conducted efficiently, ethically, and to the highest quality standards. Global Trial Managers often act as the main point of contact between sponsors, clinical sites, and regulatory authorities.

What are some common challenges faced by global trial managers when overseeing international clinical trials?

Global Trial Managers often encounter challenges related to coordinating across different countries, including navigating varying regulatory requirements, managing time zone differences, and ensuring consistent communication among global teams. Additionally, balancing the needs of local sites with the overarching project timeline can be demanding, especially when dealing with language barriers or cultural differences. Success in this role requires strong organizational skills, adaptability, and the ability to foster collaboration among diverse stakeholders.

What is the difference between Global Trial Manager vs Clinical Trial Manager?

AspectGlobal Trial ManagerClinical Trial Manager
ResponsibilitiesOversees multiple international clinical trials, manages global teams, and coordinates across regions.Manages individual clinical trials within a specific country or region, focusing on local compliance and operations.
Work EnvironmentWorks across multiple countries, often with international teams and vendors.Primarily based in one country or region, working closely with local sites and teams.
Required CredentialsTypically requires a life sciences degree, clinical research experience, and project management skills.Similar credentials: life sciences degree, clinical trial experience, and regulatory knowledge.

The main difference is that a Global Trial Manager oversees international, multi-region trials, coordinating efforts across countries, while a Clinical Trial Manager focuses on managing trials within a specific region or country. Both roles require similar qualifications but differ in scope and geographic focus.

More about Global Trial Manager jobs

What cities are hiring for Global Trial Manager jobs?

Cities with the most Global Trial Manager job openings:

What states have the most Global Trial Manager jobs?

States with the most job openings for Global Trial Manager jobs include:

Infographic showing various Global Trial 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 $130,034 per year, or $62.5 per hour.

Clinical Trial Manager

Icon plc

Philadelphia, PA • On-site

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 10 days ago


Job description

Clinical Trial Manager - Phase I oncology

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 values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.


What you will be doing

  • Manage the day-to-day operations of assigned trials and responsibilities to ensure completion per established project team goals and objectives in compliance with applicable GCP/ICH guidelines and other regulatory requirements

  • Leads or supports cross-functional trial teams, including vendors

  • Ensures accurate and up-to-date trial information within relevant tracking systems and provide regular updates of trial progression to Clinical Operations Lead, Clinical Trial Lead, and other defined stakeholders

  • Proactively identify and resolve issues that arise during trial conduct; manage escalation of trial-related issues

  • Participate in or lead the development of core trial documents, trial plans and system set-up; participate in preparation and ensure operational excellence of protocol and implementation of appropriate systems, standards, and processes to ensure quality across investigative sites, vendors, and data

  • Participate in or lead preparation of vendor requirements and project scope and selection of trial vendors; effectively manage interactions and escalations with vendor trial team

  • Participate in or lead feasibility assessment and selection of countries and sites for trial conduct

  • Participate in or facilitates site engagement and communications with investigators and/or staff to support trial milestones and deliverables

  • Oversee the clinical aspects of timely data cleaning, data analysis and the availability of top line results; participate in data reviews and review of statistical analysis plans

  • Participate in or lead set-up and implementation of effective investigator and site monitor training; coordinate operational and therapeutic area training for internal and external trial team members

  • Provide oversight and direction to trial team members for trial deliverables

  • Manage clinical trial budget and associated vendor contracts, including tracking and data in associated systems

  • Ensure quality and completeness of TMF for assigned clinical trials

  • Participates in inspection readiness activities including coordination of clinical trial team deliverables

  • Participate in the evaluation and implementation of patient-focused strategies for assigned trials, as applicable

  • Responsible for the management of budgets, timelines and resources for assigned clinical trial responsibilities


Your profile

  • BA/BS degree with at least 3 years clinical trial experience or advanced degree (MS/PhD/PharmD) with at least 2 years clinical trial management experience

  • Must have strong knowledge of ICH/GCP guidelines and regulatory requirements

  • Must have knowledge of protocol and clinical drug development processes, clinical trial design, trial planning and management, and monitoring

  • Requires project management skills and trial leadership ability

  • Must have excellent interpersonal, written and verbal communication skills, administrative skills and computer ability

  • Fluent in English

  • Experience in Phase I oncology

  • Global experience with primary focus on independent vendor set up and management, oncology cohort management and experience in supporting dose escalation safety meetings.

  • May be asked to Work East coast hours if located further West

  • Moderate (~25%) travel required


Employment with ICON is contingent upon having the legal right to work in the country where the role is based.


Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.


Benefits may include:

  • Competitive base salary and performance related incentives
  • Health and wellbeing programmes including medical, dental, and vision coverage where applicable
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programmes and wellbeing resources
  • Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.


Visit our careers site to read more about the benefits ICON offers.


Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.


If you require reasonable accommodations during the recruitment process, please let us know or submit a requesthere.

Are you a current ICON Employee? Please click here to apply