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ICON plc

Global Study Manager

Bucharest
Posted about 19 hours ago
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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.

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I’m in my final year doing Economics and I don’t know whether to apply for grad schemes now or do a masters first. What do you think?

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Graduate Consultant — 2026 Scheme

PwC·London, UK
£35,000/yr

Why you're a good match

Strong

Your economics background and your summer at a regional bank line up with what PwC looks for on the consulting scheme. Applications close in four weeks.

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Why you're a good match

You’ve got the grades and the economics background, and your bank internship is exactly the experience this scheme looks for. Apply soon — deadlines close within the month.

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Strong

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Your summer at the bank plus your econometrics coursework map directly to the day-one responsibilities on this scheme — client modelling, market briefings, and deal support.

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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 the 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.

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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.

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Skills

Clinical trial management
Clinical trial design
Regulatory compliance
Data analysis
Medical data interpretation
Project management
Cross-functional collaboration
Problem-solving
Communication
Interpersonal skills
Clinical trial protocols
Regulatory requirements
Trend identification
Stakeholder management
Clinical trial operations

Location

Sofia, Sofia-City, Bulgaria

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