ICON plc Logo

ICON plc

Global Study Manager

Posted 22 Days Ago
Be an Early Applicant
In-Office or Remote
Hiring Remotely in Northern Ireland, GBR
Senior level
In-Office or Remote
Hiring Remotely in Northern Ireland, GBR
Senior level
Lead global clinical trials end-to-end: design and implement protocols, manage day-to-day operations, ensure regulatory compliance, analyze and interpret trial data, resolve operational challenges, and coordinate internal and external stakeholders to optimize study enrollment and outcomes.
The summary above was generated by AI
Study Manager

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.


Job title - Global Study Manager/Project Manager

Location - EMEA, remote

Fully sponsor dedicated

We are currently seeking a Global Study Manager to join our diverse and dynamic team. As a Global Study Manager at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.

What you will be doing

  • Collaborate with cross-functional teams to design and implement effective clinical trial enrollment Collaborating with cross-functional teams to develop and implement comprehensive clinical trial protocols.

  • Overseeing and managing the day-to-day operations of clinical trials, ensuring compliance with regulatory standards.

  • Analyzing and interpreting clinical trial data, identifying trends, and providing insights to optimize study outcomes.

  • Proactively addressing challenges and implementing effective solutions to ensure the successful execution of clinical trials.

  • Communicating effectively with internal and external stakeholders to foster strong partnerships and facilitate smooth trial processes.

Your profile

  • Bachelor's degree in a relevant field, with a minimum of 5 years of experience in global clinical trial management.

  • Proven expertise in designing and executing clinical trials, with a strong understanding of regulatory requirements.

  • Exceptional analytical and problem-solving skills, with the ability to interpret complex medical data.

  • Effective communication and interpersonal skills, with the ability to collaborate across diverse teams.

  • Detail-oriented and organized, with a track record of successfully managing multiple tasks and priorities simultaneously.


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

Similar Jobs

5 Days Ago
In-Office or Remote
Senior level
Senior level
Healthtech
Lead complex global clinical trials from study start-up through close-out across immunology, dermatology, respiratory, and ophthalmology. Manage sponsors, cross-functional international teams, timelines, budgets, quality, risks, regulatory compliance, and operational performance while resolving issues and ensuring successful study delivery.
Top Skills: Ich-Gcp
4 Hours Ago
Remote
Expert/Leader
Expert/Leader
Artificial Intelligence • Healthtech • Machine Learning • Natural Language Processing • Biotech • Pharmaceutical
Lead design, delivery and maintenance of GMP/GDP audit strategy for biologics, aseptic, small molecule and medical device areas. Plan and execute complex audits, coach auditors, analyze regulatory intelligence, drive corrective actions, support inspection readiness, and partner with PGS/PharmSci and site stakeholders to ensure compliance and continuous improvement.
Top Skills: Aseptic ManufacturingDigital HealthEu DirectiveFdaGdpGmpIchIsoMedical Device RegulationsPic/SQuality Management SystemSoftware As A Medical Device (Samd)Tga
15 Hours Ago
Easy Apply
Remote
Easy Apply
Senior level
Senior level
Artificial Intelligence • Consumer Web • Digital Media • Information Technology • Social Impact • Software
Own product design for a major product area from opportunity identification through launch. Define problems, shape product direction, design complex multi-user flows, prototype rapidly with AI-assisted tools, and collaborate closely with product, engineering, and design leadership. Drive interaction and visual quality, influence roadmap decisions, and raise standards across the design team through feedback and shared frameworks.
Top Skills: Ai-Assisted Prototyping ToolsClaude CodeCursorFigmaLovableV0

What you need to know about the Belfast Tech Scene

If asked to name the birthplace of the RMS Titanic, you might not say Belfast. Similarly, if asked to name Europe's leading destination for foreign direct investment in new software development, Belfast might not come to mind. Yet, both are true. The city has emerged as a tech powerhouse, recently ranked among the best in the U.K. for tech careers — especially for software developers. It also leads the U.K. with the highest percentage of software development jobs advertised.

Sign up now Access later

Create Free Account

Please log in or sign up to report this job.

Create Free Account