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Global Study Manager (GSM), Hematology

ICON Plc

Location not specified

Posted: February 10, 2026

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Quick Summary

The Global Study Manager will be responsible for overseeing the global study operations, ensuring the successful delivery of clinical trials on a global level.

Job Description

Global Study Manager - Hematology
ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development
We are currently seeking an experienced Global Study Manager to join our diverse and dynamic team. As the Global Study Manager you will hold a crucial role in ensuring the successful delivery of all clinical aspects of the studies on a global level. Your expertise and leadership will be instrumental in managing the clinical portion of the budget, developing effective monitoring plans, and driving enrollment to meet project objectives. Moreover, you will liaise with stakeholders, identify and mitigate risks, and provide comprehensive reporting on all clinical activities.
The role will be managing early phase (Phase I-IIa) Hematology studies from Start up onwards. You MUST have experience in global study management, vendor management from managing multiple vendors, managing vendor budgets etc, working cross functionally and using AI as part of your day to day role
What you will be doing:
Budget Oversight Oversee the vendor portion of the budget to ensure efficient resource allocation.
Ensuring Effective Study Oversight: Develop study documents and tools, ensuring effective study oversight.
Optimizing Performance: Train and mentor junior staff
Timely Study Start-Up & Enrollment: Drive enrollment and lead study start-up activities, adhering to timelines.
Improving Study Integrity Review trip reports and implement corrective and preventative action plans when necessary.
Building Productive Relationships: Foster productive relationships with Sponsors, vendors, and cross-functional teams.

Your profile:
A minimum of 4+ years of experience in a Clinical Trial Management/ Global Study Management position at a Pharmaceutical Organization.
Bachelor's degree in health, life sciences, or other relevant fields of study.
Preferred: Early Phase (I-IIa) experience in Hematology or Oncology
Experience in managing complex or global trials is advantageous.
Preferred: Experience in managing all trial components from start-up to database lock.
Experience in using AI tools as part of your day to day tasks.
Preferred: Experience in coaching/mentoring other CTMs, leading a team of CTMs, and participating in departmental initiatives.
Fluency in English (reading, writing, speaking).
What ICON can offer you:
Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.
In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.
Our benefits examples include:
Various annual leave entitlements
A range of health insurance offerings to suit you and your family’s needs.
Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being.
Life assurance
Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others.
Visit our
careers site
to read more about the benefits ICON offers.
At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know
Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.

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