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ICON plc

Project Manager, Laboratory

Posted 3 Hours Ago
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In-Office
Singapore, SGP
Entry level
In-Office
Singapore, SGP
Entry level
Manage 10–15 clinical laboratory studies under Good Clinical Practice, serving as the sponsor’s primary contact, coordinating project delivery, attending sponsor meetings, resolving issues, developing teams, and providing progress reports while ensuring regulatory compliance and client satisfaction.
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Project Manager, Laboratory

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: Project Manager, Laboratory at Singapore Loyang office

- Office 60% and home 40%


As a Project Manager, Laboratory at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.


What You Will Do:

Your focus will be on coordinating project and programme management delivery, resolving issues, and developing team capability.
Key responsibilities include:

  • To ensure client satisfaction by acting as the Sponsor’s main contact person in all matters regarding ICON services including the day-to-day management of studies.
  • To attend and represent ICON at Sponsor meetings.
  • To manage 10-15 studies in accordance with Good Clinical Practice.
  • To communicate with Sponsor’s study progress in a responsible and professional manner and provide Sponsors with regular management reports.

Your Profile:

You will have solid project and programme management experience, with the ability to manage competing priorities and develop your team.
Required qualifications and experience:

  • Singapore citizen or permanent resident
  • Bachelor's degree in a relevant field such as life sciences or healthcare.
  • Previous experience in project management within a laboratory or clinical research setting.
  • Strong communication and interpersonal skills, with the ability to represent the company at sponsor meetings.
  • Ability to manage multiple studies concurrently while ensuring adherence to regulatory standards and guidelines.
  • Detail-oriented with strong organizational skills to effectively manage study documentation and timelines.

#LI-DP1


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

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