Global Trial Manager Remote UK
Job role insights
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Date posted
30.10.2025
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Closing date
24.11.2025
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Offered salary
Min: $1,235/month
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Career level
Senior
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Qualification
Bachelor
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Experience
6 - 9 Years
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Quantity
6 person
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Gender
Male Or Female
Description
Location: United Kingdom
ICON plc, a world-leading healthcare intelligence and clinical research organization, is seeking experienced Global Trial Managers to join our FSP group. We offer an inclusive environment that fosters innovation and excellence, with the opportunity to shape the future of clinical development.
As a Global Trial Manager, you will manage international clinical studies, collaborating with cross-functional teams and external vendors to ensure projects are delivered on time, within budget, and to the highest standards. You’ll work with innovative biotechnology companies addressing areas of unmet medical need, helping reduce the social and economic burden of disease.
Key Responsibilities:
- Lead planning and management of global clinical studies through coordination of cross-functional study teams.
- Conduct study-level risk assessments and implement risk mitigation strategies.
- Identify and resolve global study issues efficiently.
- Collaborate with Regional Clinical Trial Managers to ensure country-level study delivery aligns with global plans.
- Oversee deliverables from external partners, including CROs, labs, and imaging vendors.
- Manage study budgets, timelines, and global documentation.
- Lead development and implementation of global Drug Supply Plans.
Education & Experience Requirements:
- Bachelor’s, Master’s degree, or RN in life sciences, medicine, or related fields.
- Minimum 7 years of experience in life sciences or medically related roles.
- At least 4 years of experience in bio-pharmaceutical clinical research, preferably in biotech, pharmaceutical, or CRO companies.
- Proven experience in clinical study/project management.
- Strong experience overseeing external clinical research vendors.
- Solid project management skills including budget and timeline management.
- Experience leading cross-functional teams in a matrix environment.
- Knowledge of project risk assessment and mitigation strategies.
Ideal Candidate:
- Demonstrates strong planning and management skills for global study deliverables.
- Thrives in collaborative, fast-paced environments.
- Flexible, organized, and proactive in problem-solving.
What ICON Offers:
- Structured onboarding and comprehensive training.
- Full-time, permanent contract, home-based in the UK.
- Competitive salary package with additional allowances.
- Generous annual leave and flexible benefits.
- Health insurance tailored to your family’s needs.
- Retirement planning and life assurance programs.
- Global Employee Assistance Programme (24/7 support).
- Inclusive and accessible workplace culture.
How to Apply
If you’re interested in this position, please register on our portal and submit your application through the link below:
👉 Register & Apply at TeezJobs.com
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Yes, the role is homebased in the UK. You can work remotely, but a secure home office and reliable internet connection are required.
Q2: What are the main responsibilities?
You will plan and manage global clinical studies, lead cross-functional teams, oversee external vendors, manage budgets and timelines, and implement global drug supply plans.
Q3: What qualifications do I need?
A BA/BS/BSc or RN is required. Ideally, you have at least 7 years of experience in life sciences or clinical research, including 4 years in biotech, pharmaceutical, or CRO clinical trials.
Skills
Maps
Interested in this job?
15 days left to apply
