- Global Study Manager (GSM), CVRM
This is the employer's own posting, not a copy on a job board.
What we know
Is it still open?
Confirmed still open
Last checked 2h ago — checked against the employer's own applicant tracking system, which is the company answering directly.
We re-read the employer's own applicant tracking system and the posting was still there. That is the company answering directly.
How old is it?
Posted 17h ago
The date the source published, not the day we noticed it (2026-10-14). Last seen at its source just now.
Is it remote?
The listing says yes
The location field doesn't say remote, so our assessment is based on the title or the description. Read the listing before applying.
Who may apply?
United Kingdom
The description agrees: it names United Kingdom.
What the ad says
…UK based UK based, with 3+ years of Global trial management experience in cli…
Skills named in the ad
Recognised terms only, from a fixed vocabulary — this is what CV matching compares against.
Carried by 1 source
-
Workday employer's own board first seen 2h ago · last seen just now
- location not stated
The listing
At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise.
As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide.
About the Role
Our client is seeking a talented Global Study Manager to support the delivery of global clinical studies from protocol development through study close-out and archiving.
Working as part of a cross-functional global study team, you will collaborate with internal stakeholders, CROs, and external vendors on a global level to ensure studies are delivered on time, within budget, and to the highest quality and compliance standards. The successful candidate will have the opportunity to support innovative programmes, including global cardiovascular clinical trials focused on advancing treatments for patients with cardiovascular disease.
About You
- Degree qualified in Life Sciences, Medical Sciences, Biological Sciences, or a related field.
- UK based, with 3+ years of Global trial management experience in clinical research, pharmaceutical development, biotechnology, or a CRO environment.
- Strong understanding of clinical development and the drug development process.
- Excellent knowledge of ICH-GCP and global clinical trial regulations.
- Proven project management and organisational skills.
- Strong stakeholder management and communication skills.
- Experience working effectively within global, cross-functional teams.
- Previous experience supporting cardiovascular clinical trials is highly desirable.
- Proactive, collaborative, and able to work independently in a fast-paced environment.
Why Apply?
This is an exciting opportunity to join a leading organisation and contribute to the delivery of innovative clinical research programmes. You'll play a key role in global studies, including those within the cardiovascular therapeutic area, helping advance potential new treatments for patients living with cardiovascular disease worldwide.
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 request here.
Are you a current ICON Employee? Please click here to apply