Clinical Project Manager

ICON Strategic Solutions

Singapore

On-site

SGD 140,000 - 200,000

Full time

27 hours ago
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Benefits offered by this job

Health insurance
Annual leave entitlements
Retirement planning
LifeWorks global support programme
Life assurance
Country-specific benefits

Job summary

ICON Strategic Solutions, a sponsor-dedicated CRO, is seeking a Clinical Project Manager for Singapore/Malaysia/Thailand. You will coordinate global studies, ensuring delivery aligned with study requirements, contracts, budgets and SOPs, working with sponsors, CROs and multinational teams.

The role focuses on directing project and programme management, resolving issues and building team capability, with opportunities to contribute to proposals and bid defenses.

Qualifications

  • Bachelor’s degree in Life Sciences, Healthcare, or related field.
  • Proven experience managing clinical trials from start-up through closeout.
  • Experience leading cross-functional and multinational study teams.
  • Strong knowledge of ICH-GCP, clinical trial processes, and regulatory requirements.
  • Demonstrated ability to manage study timelines, budgets, resources, risks, and deliverables.

Responsibilities

  • Lead global cross-functional or single-service projects from initiation through closeout.
  • Coordinate project planning, execution, monitoring, and delivery across multinational teams.
  • Manage project resources and help ensure they are used effectively.
  • Maintain oversight of project timelines, contracts, budgets, and deliverables.
  • Facilitate collaboration and communication across project teams and stakeholders.
  • Support recruitment and retention activities when required.
  • Contribute project management expertise to new business proposals and Bid Defense meetings, where applicable.

Skills

Project management
Leadership
Stakeholder management
Cross-functional teams

Education

Bachelor's degree in Life Sciences/Healthcare

Job description

Clinical Project Manager - Singapore/Malaysia/Thailand

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.

As a Client Project Manager at ICON, you will take ownership of the overall direction, coordination, execution, and successful delivery of global projects. You’ll work closely with cross‑functional and multinational teams to ensure projects are delivered effectively, in line with study requirements, contracts, budgets, and applicable SOPs.

What You Will Do

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

Key Responsibilities Include
  • Lead global cross‑functional or single-service projects from initiation through closeout
  • Coordinate project planning, execution, monitoring, and delivery across multinational teams
  • Manage project resources and help ensure they are used effectively
  • Maintain oversight of project timelines, contracts, budgets, and deliverables
  • Facilitate collaboration and communication across project teams and stakeholders
  • Support recruitment and retention activities when required
  • Contribute project management expertise to new business proposals and Bid Defense meetings, where applicable
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
  • Bachelor’s degree in Life Sciences, Healthcare, or a related field preferred.
  • Proven experience managing clinical trials from start‑up through closeout. Experience in Oncology studies is highly preferred.
  • Experience leading cross‑functional and multinational study teams.
  • Strong knowledge of ICH‑GCP, clinical trial processes, and regulatory requirements.
  • Demonstrated ability to manage study timelines, budgets, resources, risks, and deliverables.
  • Strong leadership, communication, and stakeholder management skills.
  • Experience working with sponsors, CRO teams, and other clinical study stakeholders.
  • Proactive, organized, and adaptable with a strong focus on quality and study delivery.
What ICON Can Offer You

Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.

In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well‑being and work life balance opportunities for you and your family.

Our Benefits Examples Include
  • Various annual leave entitlements
  • A range of health insurance offerings to suit you and your family’s needs.
  • Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
  • Global Employee Assistance Programme, LifeWorks, offering 24‑hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well‑being.
  • Life assurance
  • Flexible country‑specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.

Visit our careers site to read more about the benefits ICON offers.

At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here

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